US20190159900A1 - Threaded composite interbody device and associated manufacturing method - Google Patents

Abstract

A composite threaded interbody device includes (a) an outer surface that is cylindrical or conical, (b) a plastic core having two outer sections, each of the outer sections forming a respective portion of the outer surface and spanning a respective azimuthal range in an azimuthal dimension relative to a longitudinal axis of the outer surface, the outer sections being separated from each other in the azimuthal dimension by two recessed sections that are recessed from the outer surface, and (c) two threaded endplates coupled to the two recessed sections and spanning gaps between the outer sections, to complete the outer surface.

Description

RELATED APPLICATIONS
• This application is a continuation of U.S. Ser. No. 15/625,965 filed Jun. 16, 2017, which is a continuation of U.S. Ser. No. 14/747,795 filed Jun. 23, 2015 (now U.S. Pat. No. 9,687,358), which is continuation of Ser. No. 13/846,818 (now U.S. Pat. No. 9,089,428), filed Mar. 18, 2013, which is a continuation of U.S. Ser. No. 13/420,206 (now U.S. Pat. No. 8,414,650) and a continuation of U.S. Ser. No. 13/420,221 (now U.S. Pat. No. 8,414,820), both filed Mar. 14, 2012, and both of which are divisionals of U.S. Ser. No. 12/697,871, filed Feb. 1, 2010 (now U.S. Pat. No. 8,303,879). The aforementioned applications are incorporated herein by reference.
BACKGROUND
• Spinal fusion treatment is considered a standard of care for intractable lower back pain arising from degenerative disc disease and/or spinal instability. Fusion includes immobilizing the painful spine segments and encouraging bone growth across the immobilized level. In the cervical spine, anterior decompression and fusion is the gold standard.
• Spine fusion was first performed without instrumentation using bone grafts, the bone grafts often being obtained from the patient's own body (i.e., from the iliac crest). Instrumented fusion, using rods, plates, and screws, was initially developed to provide rigid stability to the spine while the implanted bone grafts fused across the treated level. Since then, fusion implants have become common, replacing bone grafts.
• Conventional implants are designed to facilitate primarily through-growth, or fusion resulting from growth of bone through holes or channels through the implants, for example in order to reach other bone. For example, Medtronic LT Cages® are thimble-like titanium device that are packed with a collagen sponge soaked in rhBMP-2 (recombinant human bone morphogenic protein 2). A pair of the cages are inserted between adjacent vertebrae to initiate bone growth through the cages. Conventional CFR-PEEK cages (carbon fiber reinforced PEEK plastic cages) also rely upon through-growth—for example, the Jaguar™ and Saber™ Lumbar I/F CAGE Systems house autologous cancellous bone grafts that grow through the cages to join with adjacent vertebrae. Alphatec Novel TL spacers are made of PEEK plastic and include an internal chamber allowing for growth of bone therein.
• Although effective, through-growth occurs slowly, for example, over a period of a year or more. Through-growth can be further delayed if the implant area is not immobilized. Even micro-motion of the implant area can disturb and disrupt bone growth, leading to increased incidence of subsidence and pseudarthrosis.
• Some conventional devices attempt to improve implant stabilization by encouraging bone on-growth—a comparatively rapid, planar growth of bone upon surfaces of an adjacent implant, or upon surfaces of adjacent bone. For example, on-growth may be encouraged by coating a titanium cage with a chemical such as hydroxyapatite, a mineral naturally found in bone, to encourage new-grown bone to stick to the implant surface (for example, as is done with titanium dental implants). However, because they are radio-opaque, titanium cages and implants may hinder diagnostic assessment of bone growth, whether coated with hydroxyapatite or not. For example, implants made primarily of radio-opaque titanium may obscure visualization of bone growth (e.g., through-growth) on x-rays. Titanium may likewise cause signal artifact with MRIs or CTs, making it difficult to determine if fusion has occurred.
• In order to avoid the visualization problems of titanium implants, attempts have been made to mix hydroxyapatite with, or apply hydroxyapatite to, radiolucent PEEK plastic (or other non-scattering biocompatible material, e.g., HDPE) to form a cage/implant. However, hydroxyapatite content embrittles the material and weakens such implants. In addition, PEEK provides poorer fixation than titanium, and thus, PEEK implants must often be supplemented with posterior pedicle screw and rod instrumentation.
SUMMARY
• The interbody device described herein advances the art of fusion devices by incorporating features to encourage simultaneous on-growth, through-growth and in-growth of bone (in-growth of bone being characterized by bone growing into and around porous implant surface features). Facilitating all three types of bone growth results in faster spinal or other bony fusion. Bony on-growth onto device surfaces provides relatively quick, albeit limited mechanical rigidity. Next, in-growth, as achieved with the device described herein, incrementally increases mechanical strength as bone grows into porous features of the interbody device to anchor bone to the device. Finally, bony through-growth, which takes the longest to complete, fully stabilizes and completes the fusion. On-growth and in-growth enhance device stabilization, thus accelerating complete fusion by minimizing micro-motion that could disrupt through-growth.
• The interbody device described herein is primarily discussed in terms of a PEEK plastic core or preexisting interbody device (such as an artificial disc) with metallic endplates. Titanium endplates are discussed in depth; however, it will be appreciated that other biocompatible metals, as well as alternate core or preexisting device materials, may fall within the scope hereof.
• In one embodiment, a composite interbody device includes a plastic core with superior and inferior surfaces and one or more features for permitting bone growth through the core. A superior endplate has a core interface side coupled with the superior surface. The superior endplate has a bone interface side opposite the core interface side, for interfacing with bone of an implant site. The bone interface side includes multiple bone interface pores for permitting bone growth therein. A metallic inferior endplate includes a core interface side and a bone interface side opposite the core interface side. The core interface side couples with the inferior surface of the core. The bone interface side interfaces with bone of an implant site and includes bone interface pores for permitting bone growth therein. A hydroxyapatite coating applied to the bone interface sides of the superior and inferior endplates encourages bone growth onto the endplates.
• In another embodiment, a composite interbody device includes a superior endplate, an inferior endplate and a core between the superior and inferior endplates. The superior endplate and the inferior end plate each have a hydroxyapatite-coated, porous bone interface side for contacting bone of an implant site. The hydroxyapatite coating encourages bone growth onto the bone interface side, and pores of the bone interface side permit bone growth into the bone interface side. The superior and inferior endplates each have a porous core interface side opposite the bone interface side, a central barrier layer between the core interface side and the bone interface side; and at least one aperture through the endplate. The plastic core has a superior surface bonded with and penetrating pores of the superior endplate core interface side; and an inferior surface bonded with and penetrating pores of the inferior endplate core interface side. At least one channel through the core is aligned with the superior endplate aperture and with the inferior endplate aperture, the channel thus providing a pathway for through growth of bone through the interbody device.
• In another embodiment, a composite interbody device has a plastic core with superior and inferior surfaces and one or more features for permitting bone growth through the core. A superior endplate includes a core interface side configured with the superior core surface, and a bone interface side opposite the core interface side, for interfacing with bone of an implant site. The bone interface side is coated with hydroxyapatite and has multiple micro-machined surface features for increasing the bone interface side surface area to enhance bonding between bone and the superior endplate. An inferior endplate has a core interface side configured with the inferior core surface and a bone interface side opposite the core interface side for interfacing with bone of an implant site. The bone interface side is coated with hydroxyapatite and has multiple micro-machined surface features for increasing the bone interface side surface area to enhance bonding between bone and the inferior endplate.
• In another embodiment, a method of manufacturing a composite interbody device includes assembling superior and inferior endplates by forming a solid central barrier layer on a bone interface layer, opposite a bone interface side of the bone interface layer. A porous core interface layer is formed on the central barrier layer opposite the bone interface layer. The inferior and superior endplates are placed in a mold, on each side of a core cavity, with the core interface layers facing the core cavity and the bone interface sides facing away from the cavity. Molten plastic is injection-molded into the core cavity, to form a plastic core between the endplates and bonded with core interface sides of the core interface layers. The molten plastic extrudes into pores of the core interface layers to bond with the endplates.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective view of a composite interbody device with superior and inferior endplates, according to an embodiment.
• FIG. 2 is a cross-sectional view through the interbody device ofFIG. 1.
• FIG. 3 is a side view of the interbody device ofFIG. 1.
• FIG. 4 is a top view of the interbody device ofFIG. 1.
• FIG. 5 is a top view of the superior endplate ofFIG. 1, showing a bone interface side.
• FIG. 6 is a side view of the superior endplate ofFIG. 5.
• FIG. 7 is a bottom view of the superior endplate ofFIG. 65, showing a core interface side.
• FIG. 8 is a perspective view of the superior endplate ofFIG. 5.
• FIG. 9 is a bottom view of the inferior endplate ofFIG. 1.
• FIG. 10 is a side view of the inferior endplate ofFIG. 9.
• FIG. 11 is a top view of the inferior endplate ofFIG. 9, showing a core interface side.
• FIG. 12 is a perspective view of the inferior endplate ofFIG. 9.
• FIG. 13 is a schematic view of a bone interface layer of the superior or the inferior endplate ofFIG. 1.
• FIG. 14 is an enlarged view of an area of the bone interface layer ofFIG. 13.
• FIG. 15 is a schematic view of a core interface layer of the superior or the inferior endplate ofFIG. 1.
• FIG. 16 is an enlarged view of a section of the core interface layer ofFIG. 15.
• FIG. 17 is a sectional view through the core interface layer ofFIG. 15.
• FIG. 18 is an enlargement of a portion of the sectional view ofFIG. 17.
• FIG. 19 is an exploded view showing layers forming an endplate ofFIG. 1, according to an embodiment.
• FIG. 20 is a top view of the endplate ofFIG. 19, showing an outermost bone interface layer.
• FIG. 21 is a sectional view through the endplate ofFIGS. 19 and 20.
• FIG. 22 is an enlargement of a portion of the sectional view ofFIG. 21.
• FIG. 23 is an exploded view of a composite interbody device having machine-featured superior and inferior endplates, in accordance with an embodiment.
• FIG. 24 is a perspective view of the composite interbody device ofFIG. 23, as assembled.
• FIG. 25 is a side view of the assembled interbody device ofFIG. 24.
• FIG. 26 is a bone-side view of the superior or inferior endplate ofFIGS. 23 and 24.
• FIG. 27 is an insertion end view of the device ofFIG. 24.
• FIG. 28 is an exploded perspective view showing composite layers forming the endplates ofFIG. 1 as applied to an artificial disc, according to an embodiment.
• FIG. 29 is a flowchart showing a method of forming an interbody device, according to an embodiment.
• FIG. 30 is a flowchart illustrating another method of forming an interbody device, according to an embodiment.
• FIG. 31 is a flowchart showing a method of forming an interbody device, according to an embodiment.
• FIG. 32 is a flowchart showing a method of forming an interbody device, according to an embodiment.
• FIG. 33 is a flowchart illustrating a further method of forming an interbody device, according to an embodiment.
• FIG. 34 is a simplified exploded, perspective view of a composite interbody device with superior and inferior endplates, according to an embodiment.
• FIG. 35 is an end view of the device ofFIG. 34.
• FIG. 36 is a perspective view of the superior endplate ofFIG. 39.
• FIG. 37 is an end view of the endplate ofFIG. 41.
• FIG. 38 is a top view of the endplate ofFIG. 36.
• FIG. 39 is an enlarged view of a section of the endplate shown inFIG. 38.
• FIG. 40 is perspective view of the assembled device ofFIG. 34, including post-assembly, machined features, according to an embodiment.
• FIG. 41 is an exploded view of the device ofFIG. 40.
• FIG. 42 is a side view of the device ofFIG. 40.
• FIG. 43 is a top view of the device ofFIG. 40, showing additional detail of a superior endplate.
• FIG. 44 is an enlarged view of a section of the device shown inFIG. 43.
• FIG. 45 is a perspective view of a composite interbody device having superior and inferior endplates, according to an embodiment.
• FIG. 46 is a second perspective view of the device ofFIG. 45.
• FIG. 47 is an exploded view of the device ofFIGS. 45-46.
• FIG. 48 is a side view of the device ofFIGS. 45-47.
• FIG. 49 is a cross-sectional view through the device ofFIG. 48.
• FIG. 50 is a top view of the superior endplate of the device ofFIGS. 45-47, showing a bone interface surface.
• FIG. 51 is an end view of the device ofFIGS. 45-47.
• FIG. 52 is a side view of the device ofFIGS. 45-47, showing a lateral channel for bone through-growth.
DETAILED DESCRIPTION
• FIG. 1 shows acomposite interbody device100 including asuperior endplate102 and aninferior endplate106, flanking acore104.Core104 is for example a PEEK core (i.e., injection molded thermosetting PEEK plastic) having one or more features108, such as channels throughcore104, for encouraging bone growth throughdevice100, and/or for housing a fusion enhancing material such as bone and any associated growth enhancers, or a fusion enhancing glue.Core104 may alternately be made of any other biocompatible material that is sufficiently malleable for forming in a desired shape, yet strong enough to meet durability requirements of an intended implant site. Features108 may be machined aftercore104 is injection molded, or features108 may be extruded or otherwise formed.Feature108A is a vertically-oriented channel that runs top-to-bottom throughcore104, which aligns with anaperture110 insuperior endplate102 and anaperture112 throughinferior endplate106, whenendplates102 and106 are assembled withcore104. Alignment ofaperture110,channel108A andaperture112 together form a passage that allows bone growth entirely throughdevice100. Because PEEK is radiolucent,core104 may include one ormore radio markers114 for facilitating visualization ofcore104 on x-ray during or after implantation.
• Feature108B is a horizontally-oriented aperture or hole in a side ofcore102, or alternately, a channel that runs side-to-side throughcore104. Feature108C (labeled inFIG. 2) is a horizontally-oriented aperture or hole in a back side (distal to the spinal cord when inserted between vertebrae) ofcore104, or alternately, a channel that runs back-to-front throughcore104. In one embodiment, features108B and108C open into vertically-orientedchannel108A, thus permitting bone growth through the sides and back ofdevice100, in addition to vertical bone growth through channel108 andendplate apertures110 and112.Features108A-C may be created by machining aftercore104 is molded (e.g., after injection-molding core104 betweenendplates102 and106. Alternately, features108A-C may be molded intodevice100 by use of one or more removable mandrels placed in a mold for formingdevice100.
• As shown,endplates102/106 are curved to conform to an accepting bony surface, as further described with respect toFIG. 3, below. Whencore104 is molded betweenendplates102 and106,device100 for example assumes a bullet shape that facilitates insertion into an implant site. It will be appreciated thatendplates102 and106 may be straight, curved, angulated or otherwise shaped, depending upon the intended application (i.e., the intended implant site or intended final shape of device100).Endplates102 and106 are for example diffusion bonded in a press, to achieve a desired shape and/or contour.
• Endplates102/106 are for example porous titanium coated with hydroxyapatite (HA), to encourage both bone on-growth (onto the porous endplates) and in-growth (into pores of the endplates). Coating titanium endplates, rather than a PEEK core directly, with HA promotes bioactivity (e.g., bone growth) without sacrificing strength and toughness ofcore104. Titanium is a biocompatible material that bonds with HA and therefore facilitates bone on-growth withendplates102 and104. Titanium HA coated endplates provide strength, biocompatibility and on-growth without compromising the strength of the PEEK core as occurs when HA is blended directly into PEEK (PEEK fracture toughness is known to be degraded with direct application of HA). In addition, the titanium-PEEK-titanium combination ofdevice100 avoids the greater stiffness of a primarily titanium implant, thereby reducing stress shielding that inhibits bone growth and bone fusion. It will be appreciated that other biocompatible metals such as molybdenum, cobalt-chrome, stainless steels and other biocompatible alloys, may be used in place of or in addition to titanium in formingendplates102 and106. For example other biocompatible metals may be alloyed with titanium to formendplates102 and106.
• FIG. 2 is a rear view ofdevice100, featuringendplates102 and106 configured withcore104 and showing rear feature108C. Rear feature108C is an aperture incore104 having dimensions of about 4 mm wide by 3-6 mm high. In addition to permitting bone growth through the back end ofcore104, feature108C facilitates placement ofdevice100 at an implant site by use of a tool sized to fit feature108C.
• In one aspect, height (h_D) ofdevice100, includingendplates102 and106, ranges from about 12 mm to about 17.1 mm. When aligned withchannel108A,aperture110 ofsuperior endplate102 andaperture112 ofinferior endplate106 may open into common space withincore104, which is also accessible via at least feature108C.
• FIG. 3 is a side view of assembleddevice100. In one aspect,device100 includes superior and inferiorendplate contact surfaces116 and118, spanning at least a portion of the length (l_D) ofdevice100/core104. Length l_Dis for example about 26 mm.Endplates102/106 are curved to conform with a shape of contact surfaces116 and118. Although not shown inFIG. 3, it will be appreciated thatendplates102 and106 may also be shaped on bone interface sides126, opposite the endplate contact surfaces, to conform or optimally interact with bony surfaces of an intended insertion site.Core104 may be beveled starting at abevel line120 to anose122, to facilitate insertion between bony surfaces such as adjacent vertebrae.Device100 is for example inserted nose-first between vertebrae in the direction indicated byinsertion arrow124.Endplates102/106 have an endplate height (h_E) of between about 1-2 mm.Endplates102/106 may be coated with hydroxyapatite before or after assembly withcore104. In one example,endplates102/106 are spray coated with hydroxyapatite prior to placement in a mold, andcore104 is injection molded betweenendplates102/106.
• FIG. 4 is a simplified top view ofdevice100 showingbone interface side126 ofsuperior endplate102, described further with respect toFIGS. 5-8. It will be appreciated, after reading the following description, thatFIG. 4 may also represent a bone interface side ofinferior endplate106.
• In an embodiment according toFIGS. 4-8,device100 width (w_D) is about 11 mm.Aperture110 ofendplate102 has an aperture length (l_A) of about 13-14 mm and an aperture width (w_A) of about 5-6 mm (FIG. 4).Endplate102 has a superior endplate length (l_ES) of about 22-23 mm (FIG. 5).Bone interface side126 ofendplate102 is for example HA-coated titanium, molybdenum or other biocompatible metal, which includes a plurality of holes orpores127 into which bone may grow whendevice100 is implanted.Bone interface side126 is opposite a core interface side128 (FIG. 6).Core interface side128 facescore104 and includes a plurality of holes orpores129 for accepting material ofcore104 to enhance adhesion tocore104.Pores127 ofbone interface side126 are of optimal size for promoting bone in-growth. For example, pores127 are about 600 microns in diameter.Pores129 ofcore interface side128 are larger than thepores127 ofbone interface side126, to maximize bonding betweencore104 andendplate102. When injection molded betweenendplates102 and104,core104 material penetratescore interface side128 via thelarger pores129, to firmly bondendplate102 withcore104.Pores127 and129 may be perforations or holes throughsides126 and128, respectively, or pores127 and129 may be openings in a wiremesh forming sides126 and128. The terms pores, perforations and openings are used interchangeably, below.
• Superior endplate102 andinferior endplate106 are curved or otherwise shaped for ease of insertion. However,endplates102 and106 may alternately be shaped to maximize contact betweendevice100 and adjacent bone (for example, endplate bone-interface sides126 may be flattened to maximize surface area contact betweenendplates102/106 and adjacent bone). As shown inFIGS. 1, 3, 8 and 12,endplates102 and106 are curved to mate with accepting vertebral surfaces at an implant site. The shape ofdevice100 therefore mimics an intervertebral space. Shape and size ofdevice100 andendplates102/106 and/orcore104 may be altered to suit differently sized and shaped implant sites.Device100 may be shaped to mimic a cavity created by a cutting tool used to prepare an implant site. For example,device100 may be shaped to mimic a cavity reamed out by a ball mill to facilitate fusion at a hip, knee or shoulder joint.
• FIGS. 9-12 show additional detail ofinferior endplate106, and are best viewed together with the following description. Likeendplate102,endplate106 has abone interface side126 with pores127 (that are for example about 600 microns) and acore interface side128 with relativelylarger pores129 for acceptingcore104 material.Bone interface side126 may be hydroxyapatite-coated titanium, molybdenum or other biocompatible metal.Aperture112 may be created by machining after molding, and is sized to permit access to vertically-orientedchannel108A ofcore104, for example having dimensions similar toaperture110 ofsuperior endplate102.Endplate106 may be slightly shorter thanendplate102, having an inferior endplate length (l_EI) of about 21-22 mm.Endplates102/106 are, for example, fabricated from a large sheet ofbone interface side126 material backed bycore interface side128 material that is cut into multiple endplates, which are then shaped as desired. For example, sheets ofcore interface side126 material andbone interface side128 material may be preliminarily bonded and cut into desired sizes for formingendplates102/106. The cut sections may then be diffusion bonded to permanently joinside126 material withside128 material at a molecular level, under heat and pressure.Endplates102/106 may be curved or otherwise shaped as desired during or prior to diffusion bonding. As described below with respect to endplate assembly200 (FIG. 19), a central barrier layer is inserted betweenside126 material andside128 material, to prevent core material that penetratespores129 ofcore interface side128 from seeping into or clogging bone in-growth areas provided bypores127 ofside126.
• FIG. 13 is a top view ofbone interface side126 ofendplate102/106, andFIG. 14 shows additional detail of a section A ofside126. In one embodiment,bone interface side126 is a thin sheet of titanium, and pores127 are perforations throughbone interface side126.Perforations127 have a diameter of about 0.30 mm and a center-to-center spacing of about 0.050 mm along a givenrow130 or132. For example, a distance from the center ofperforation127A to the center ofperforation127B inrow132 is about 0.30 mm.Perforations127 ofadjacent rows130 and132 are offset such that a center-to-center (diagonal) distance betweenperforation127A inrow132 andperforation127C inrow130 is about 0.030-0.045 mm.Perforations127 may commence about 0.030-0.040 mm from edges ofbone interface side126.
• As illustrated inFIGS. 15-18, in one embodiment, pores129 ofcore interface side128 are perforations through a thin sheet of titanium or other metal.Perforations129 are optimized for accepting material ofcore104 whencore104 is injection molded betweencore interface sides128 ofendplates102/106.Perforations129 are larger thanpores127, and may be elliptical to rectangular in shape. In one aspect,perforations129 have a width (w_P) of about 0.050 mm and a length (l_P) of about 0.100 mm.Perforations129 are for example spaced at about 0.050 mm from edges ofside128 and adjacent perforations are spaced about 0.010 mm apart.
• FIG. 17 is a cross-sectional view ofside128, taken along line17-17 ofFIG. 15.FIG. 18 is an enlarged view of section B ofFIG. 17, showing a side view ofperforations129.
• FIG. 19 is an exploded view of anassembly200 for formingendplate102 and/orendplate106 ofinterbody device100, described above.FIG. 20 illustrates a bone interface side view ofassembly200.FIG. 21 is a cross-sectional illustration taken along line21-21 ofFIG. 20, andFIG. 22 is an enlarged view of a portion C ofFIG. 21, showing additional detail ofassembly200 in cross-section.FIGS. 19-22 are best viewed together with the following description.
• In an embodiment according toFIGS. 19-22,assembly200 includes abone interface side202 including at least two bone interface layers204 and206. First and second bone interface layers204 and206 are shown inFIG. 19. Additional bone interface layers (e.g., for a total of four to five layers) may be added, to vary bone in-growth characteristics ofside202 and/or tensile strength or other characteristics ofendplate102 or106 formed fromassembly200.
• First andsecond layers204 and206 are for example coated with hydroxyapatite to encourage bone on-growth, and are formed of titanium wire mesh of an optimal size for bone in-growth (e.g., the mesh providespores208 of about 600 microns diameter). The wire of the mesh is for example 0.5 mm titanium wire, and provides relatively low porosity and relatively high flow restriction as compared with a core interface side210.Pores208 may alternately take on a square, rectangular or other shape having minor dimensions of about 600 microns (e.g., the width of a rectangular pore) and major dimensions of no more than approximately three times the minor dimensions (e.g., the rectangular pore is no longer than about 1800 microns).
• Core interface side210 lies oppositebone interface side202 and includes at least onecore interface sheet212 of titanium or other biocompatible metal.Sheet212 includes perforations or pores214 that are larger thanpores208 ofside202, to maximize bonding between an endplate formed withassembly200 and an interbody core such ascore104, or another interbody device, such as an artificial disc.
• Core interface sheet212 may be a mesh formed with larger-gauge wire than the mesh oflayers204 and206, or with a looser-weave mesh to provide relatively larger pores, higher porosity and lower flow restriction thanside202. Higher porosity and lower flow restriction enhance flow of material from an interbody core/device (i.e.,core104 material) intopores214 of side210, to encourage bonding between an endplate (i.e.,endplate102/106) formed withassembly200 and the core/device. It will be appreciated that although asingle sheet212 makes up core interface side210 inFIG. 19, side210 may includemultiple sheets212 of larger-gauge titanium wire mesh.
• Alternately, side210 includes one or more perforated or micro-etchedcore interface sheets212 with pores sized to encourage bonding between an endplate (e.g.,endplate10/106) formed withassembly200 and an interbody core/device. A central plate orlayer216 between side202 (layers204 and206) and side210 (sheet212) prevents material from the interbody core/device (e.g., PEEK of core104) from over-extruding intoendplate102/106.Central layer216 for example prevents PEEK orother core104 material from flowing all the way throughendplate102/106, blocking the plastic from flowing into bone interface layers204 and206 and thus maintaining the bony in-growth spaces provided bypores208.
• Assembly200 is diffusion bonded, by placinglayers204,206,212 and216 into a die and applying heat and pressure to create an artificial porous matrix. Diffusion bonding at an atomic level facilitates combination of surfaces that touch one another, and results in near 100% bonding. Diffusion bonding may occur prior to formingendplates102/106 fromassembly200. For example,assembly200 may be formed as a 50 mm by 25 mm by 0.75 mm composite sheet (or an alternately sized composite sheet), andendplates102/106 may be cut fromassembly200 after diffusion bonding. Alternately,endplates102/106 are cut from assembly200 (which may be preliminarily bonded) orassembly200 is sized to the requirements ofendplates102/106, prior to diffusion bonding. Since diffusion bonding does not require flat sheets, unique curvatures of either or bothendplates102/106 are accommodated. Curvature may be integrated into dies for diffusion bonding to allow customization ofendplates102/106 for any interbody device/core (such as core104) and/or any accepting bony surface. For example,endplates202 and206 may be diffusion bonded in a press to produce a desired endplate shape or contour. During manufacture,endplates102/106 may also be mirrored or trimmed to suit multiple sizing requirements.
• In one embodiment,dual assemblies200 are sized according to sizing requirements forendplates102 and106.Assemblies200 are positioned into a mold with core interface sides210 facing a cavity for core material (e.g.,core104 material or material for forming an artificial disc or another interbody device configured for bonding withendplates102/106). Core material (e.g., PEEK) is injection molded betweenassemblies200 and penetratespores214 of core interface side210, to firmly bond with assembly200 (endplates102/104).Central layer216 prevents core material from over-extruding intopores208 oflayers204 and206, thus preserving bone in-growth spaces ofbone interface side202. As shown inFIG. 22,pores208 oflayers204 and206 may be selectively offset to optimizeside202 for bone in-growth.
• Once set, the shape and geometry of the interbody core/device (e.g., core104) may be refined by machining out of composite blanks. For example, features108 are machined intocore104 after molding (seeFIG. 1). Hydroxyapatite is surface treated ontobone interface side202 ofendplates102/106, before or aftercore104 is injection molded therebetween, to promote bone on-growth and in-growth onto and intobone interface side202. Hydroxyapatite may be spray-coated, painted or otherwise applied to bone interface sides202. Depth of the hydroxyapatite coating may be varied to achieve optimal on-growth/in-growth efficiency, or according to an intended implant location. The metal-PEEK-metal (e.g., titanium-PEEK-titanium) combination ofdevice200 is less stiff than a primarily titanium implant and thus reduces stress shielding.
• In one embodiment, titanium sheets formed with perforations and/or texture replace the mesh forming one or both oflayers204 and206.Layers204 and206 may be selectively micro-perforated or photo etched to providepores208 and/or other texturizing features. For example, layers202 and204 are etched with 500 micron (40-mil) perforations/pores208 using a photo etching process capable of a resolution of 5 mil (0.125 mm).Side202 may thus be formed as a matrix of sequentially stacked titanium perforations/pores208. Selective placement of titanium perforations/pores208 onside202 andlarger pores214 on side210 allows porosity control for regulating/encouraging both bone in-growth and PEEK bonding. For example, porosity may be controlled to producepores208 of approximately 500-600 microns, for ideal bone in-growth.
• FIGS. 23-26 show aninterbody device300 having machine-featured superior andinferior endplates302 and306, flanking acore304.Core304 may be similar tocore104 ofFIG. 1.Core304 includes multiple features308, such as vertically-orientedchannel308A running top-to-bottom throughcore104, and a horizontally-orientedchannel308B running side-to-side throughcore104.Features308A and308B facilitate bone growth throughcore304/device300, and may be packed with bone and/or other materials to enhance fusion (e.g., proteins or other materials to enhance bone growth, or fusion enhancing glues). Aslot308C in a back side (distal to the spinal cord when inserted between vertebrae) ofcore304 is sized to fit an insertion tool, to facilitate insertion ofdevice300 between adjacent vertebrae.Features308A-C may be machined aftercore304 is molded (e.g., after injection-molding core104 betweenendplates302 and306) or features308A-308C may be extruded or otherwise formed.
• Channel308A aligns with anaperture310 insuperior endplate302 and with anaperture312 ininferior endplate306 whendevice300 is assembled as shown inFIG. 24. It will be appreciated that any fusion aids for insertion intodevice300 may be loaded viaaperture310 oraperture312. Wherecore304 is formed of radiolucent material, such as PEEK plastic, one ormore radio markers314 may be incorporated to facilitate visualization ofcore304 on x-ray, for example oncedevice300 is implanted.Endplate302 bonds with a superiorendplate contact surface316 ofcore304, andendplate306 bonds with an inferiorendplate contact surface318, as shown inFIG. 25.Core304 may taper from abevel line320 to anose322, to facilitate insertion ofdevice300 into an intervertebral space or other implant site.
• Endplates302 and306 are curved as a result of forming and diffusion bonding in a press to conform to a desired shape ofcore304 and/or an accepting bony surface. In one aspect,endplates302 and306 are multi-surface machined yielded titanium plates with geometric features protruding therefrom, to increase relative endplate surface area for bone on-growth on bone interface sides326 (seeFIG. 25).Ridges313 are shown inFIGS. 23-27 for ease of illustration; however, it will be appreciated thatridges313 are representative only and may be replaced or supplemented by thin webs or other geometries. For example,endplates302 and306 may bear geometric features resulting from fracturing (i.e., pulling apart) a titanium plate. Such endplates may advantageously be formed in a one-step manufacturing process, thereby reducing overall cost of the interbody device.
• Alternately, although not shown,core interface sides328 ofendplates302 and306 may also bear geometric features for increasing surface area ofcore interface sides328 to enhance bonding withcore304 material. Alternately, a porous titanium layer, such as sheet212 (seeFIG. 19) may be diffusion bonded with a back (un-featured) surface of a single titaniumsheet having ridges313 or other features on its opposite side. For example,core interface side328 may include a sheet of titanium wire mesh or perforated titanium that is diffusion bonded with a back surface ofbone interface side326. In such configuration, no central barrier layer is required.
• Device300 length (l_D300) and height (h_D300), shown inFIG. 25, are for example similar to length (l_D) and height (h_D) of device100 (seeFIGS. 2-3).Device300 width (w_D300), shown inFIG. 26, may also be similar to width (w_D) ofdevice100.
• FIG. 28 is an exploded perspective view of aninterbody device400, showing composite layers forming superior andinferior endplates402 and406, as applied to anartificial disc404. In one embodiment,endplates402 and406 each include bone interface layers405 and407 selectively placed, one layer relative to the other, to optimize bone in-growth spaces provided by pores orperforations408 oflayers405 and407. Adisc interface layer412, having relatively larger pores414 (as compared with pores408), is separated fromlayers405 and407 by acentral barrier layer416 that is for example a thin sheet of solid metal. Larger pores416 admit flow ofartificial disc404 material therein. For example, molten or softenedplastic forming disc404 may extrude intopores414 to maximize contact and bonding betweendisc404 andlayer412, and thus betweendisc404 andendplates402 and406.Central barrier layer416 prevents material ofdisc404 from flowing intopores408, thus reservingpores408 for bone in-growth.
• Bone interface layers405 and407,disc interface layer412 andcentral barrier layer416 are made of a biocompatible metal such as titanium. In one embodiment, bone interface layers405 and407 are HA-coated titanium wiremesh having pores408 formed by spaces between small gauge (e.g., 0.5 mm) titanium wire. However, a perforated, HA-coated titanium sheet may replace one or both of bone interface layers405 and407.Central barrier layer416 is a solid sheet of titanium, andcore interface layer414 is a sheet of titanium mesh having larger pores than bone interface layers405 and407, to enhance bonding withartificial disc404.
• Endplates402 and406 may be applied layer-by-layer to superior and inferiorendplate contact surfaces417 and418 ofcore404. For example,disc interface layer412 is first applied to superiorendplate contact surface417.Central barrier layer416 is applied tolayer412, and titanium/HA bone interface layers407 and405 are applied tocentral barrier layer416.Layers405 and407 may be selectively placed to optimize interface between sheets, and to optimize porosity (i.e., alignment ofpores408 of eachlayer405,407) for bone in-growth. Although not shown, layers405 and407 may themselves each include multiple sublayers (e.g., 4-5 sublayers) of titanium wire mesh to provide further lower porosity and raise flow restriction. Contact surfaces417 and418 may be PEEK plastic, titanium, cobalt chrome or alloy surfaces ofartificial disc404, the remainder of which may be configured of the same material or an alternate material as contact surfaces417 and418. Any of bone interface layers405,407 andcentral barrier layer416 may be diffusion bonded to one another or todisc interface layer412. Whereartificial disc404 includes metallic contact surfaces417 and418, all layers ofendplates402 and406 may be diffusion bonded directly to the metallic contact surfaces.
• Artificial disc404 may also be molded betweenpre-assembled endplates402,406, as described above with respect tocore104 ofinterbody device100.
• Layers405,407,416 and412 may optionally be pre-formed into singlecomposite endplates402/406 that are shaped (i.e., via simultaneous forming and diffusion bonding in a press) to complement respective contact surfaces417 and418, and that are applied in single operations to superiorendplate contact surface417 and to inferiorendplate contact surface418. One exemplary disc suitable for application oflayers405,407,416 and412 (orendplates402/406 formed therefrom) is a Pioneer NuBak PEEK on PEEK disc.Endplates402 and406 may be shaped to compliment a shape of disc surfaces417 and418, ordisc404 may be injection molded between the endplates, withdisc404 conforming to the shape of the endplates.
• FIG. 29 illustrates onemethod500 for forming an interbody device, such asdevice100. Inferior and superior endplates are assembled, instep502, and placed in a mold with core interface layers facing a core cavity, instep504. Core material is injection molded into the cavity and, through the cavity, into pores of the core interface side, instep506. In one example of steps502-506,endplates102 and106 are assembled as described with respect toFIG. 19 (assembly200). The endplate-core-endplate assembly is allowed to set (for example, the assembly may be cooled until the core fully hardens), instep508, and removed from the mold, instep510. Features are formed in the interbody device, instep512. In one example ofstep512, features108A-108C andapertures110 and112 are formed indevice100. For example, one channel may be drilled throughdevice100 to formaperture110,channel108A andaperture112. Bone interface surfaces of the device (i.e., bone interface surfaces126, seeFIG. 3) are coated with hydroxyapatite, instep514. It will be appreciated that although shown as a final step inFIG. 29, hydroxyapatite may alternately or additionally be coated onto bone interface surfaces prior to their incorporation intoendplates102 and106, or after formation of the endplates and prior to placement in the mold.
• FIG. 30 shows amethod600 for forming an interbody device.Method600 is for example used to formdevice100, with an assembly such asassembly200 used to formendplates102 and106. A central barrier layer is formed on a core interface side, instep602, and a bone interface side formed on the central barrier layer, opposite (e.g., on an opposite side from) the core interface side, instep604. In one example of steps602-604,central layer216 is placed on core interface side210, andbone interface side202 is placed on central layer216 (FIG. 19). If shaping is required (decision606), for example if endplates such asendplates102 and106 are to be cut from a larger assembly ofsides202 and210 andcentral layer216, then endplates are shaped from the assembly, instep608. The endplates are diffusion bonded, in step610, and placed into a mold with core interface sides facing a cavity, instep612. In one example of steps606-612,endplates102 and106 are cut from a larger master sheet of preliminarily bondedside202,central layer216 and core side210, and diffusion bonded under heat and pressure, prior to placement in a mold having a cavity sized and shaped for formingcore104. In another example, a master sheet ofside202,central layer216 and core side210 is diffusion bonded prior to cutting or otherwise shapingendplates102 and106 from the master sheet. The endplates are then placed into a mold as described.
• Instep614, core material is injection-molded into the core cavity, and allowed to extrude into pores of the core interface side. The molded assembly is allowed to set until hardened, instep616, and removed from the mold, instep618. Endplate and/or core features may be created in the hardened interbody device, instep620. In one example of steps614-620, material ofcore104, such as molten PEEK plastic, is injection molded into the core cavity and allowed to extrude into perforations or pores214.Central barrier layer216 prevents thecore104 material from extruding intopores208 ofside202, thus reservingpores208 as bone in-growth spaces. Once hardened,apertures110 and112 may be formed in superior andinferior endplates102 and106 (respectively), andchannel108A, channel108B and aperture108C may be formed incore104. For example,apertures110 and112 andchannel108A may be formed in a single drilling or other machining operation throughinterbody device100. Optionally, certain features ofcore104 may be produced via a specially shaped mold having one or more mandrels for producing passages in the molten PEEK plastic.
• FIG. 31 illustrates amethod700 of forming an interbody device, such asdevice100, the endplates of which may be formed fromassembly200. Instep702, titanium wire mesh is selectively layered to form a bone interface side. A central barrier layer is formed from a solid titanium sheet, on the bone interface side, and a core interface layer is formed from larger-weave titanium mesh, on the central barrier layer, insteps704 and706. In one example of steps704-706,bone interface side202 is formed by selectively placing together titanium wire mesh layers204 and206, such that thepores208 formed by openings in the mesh are at a desired orientation, one layer relative to the other.Central layer216, which is for example a solid titanium sheet, is placed withside202, and at least onecore interface sheet212 is placed with the opposite side ofcentral layer216, to form bone interface side210. As noted above, pores214 ofsheet214 are larger thanpores208, to reduce flow restriction on the core interface side.
• The bone interface side, barrier layer and core interface side (e.g.,side202,central layer216 and side210) are diffusion bonded together, in step708. If shaping is required (decision710), endplates (e.g.,endplates102 and106) are shaped from the bone interface side/barrier layer/core interface side assembly, instep712, and optionally coated with hydroxyapatite on their bone interface sides, in step714. Step714 is illustrated as a dotted box to indicate that hydroxyapatite coating may take place at other points inmethod700, for example atposition726 or elsewhere.
• The endplates are placed in a mold with their bone interface sides facing a core cavity, instep716, and core material is injection molded between the endplates, and allowed to extrude into the pores (e.g., mesh openings) in the core interface side, instep718. After setting (Step720), the interbody device is removed from the mold, instep722, and endplate and/or core features are created, inoptional step724. In one example of steps716-724,endplates102 and106 are placed into a mold with sides210 facing an adjacent cavity. Molten material of core104 (e.g., PEEK plastic) is injected into the mold and allowed to penetratepores214. After the PEEK is allowed to set, the rough interbody device is removed from the mold, andapertures110 and112 are formed inendplates102 and106, and any offeatures108A-108C that were not formed inmolding104 are machined intocore104. For example,apertures110,112 andchannel108A are drilled throughdevice100.
• Bone interface sides (e.g., sides202) are coated with hydroxyapatite after the interbody device is machined with its desired features, after the endplates are shaped from the bone interface side/barrier layer/core interface side assembly, or both. Alternately, mesh layers forming the bone interface side may be coated with hydroxyapatite prior to placing the layers together to form the bone interface side, or the bone interface side may be coated with hydroxyapatite prior to its placement with the central barrier layer. The depth and placement of hydroxyapatite coating may vary as a function of an intended implant site.
• FIG. 32 illustrates amethod800 of forming an interbody device.Method800 may be used to formdevice100 usingassembly200 to makeendplates102 and106. A bone interface side is formed from at least one sheet of perforated titanium, in step802, and a central barrier layer formed from a solid sheet of titanium is placed on the bone interface side, in step804. A core interface side is formed on the central barrier layer, opposite the bone interface layer, instep806. In one example of steps802-806,bone interface side202 is formed by selectively placing a plurality of perforated titanium sheets together such that the perforations are at a desired orientation, one layer relative to the other. See alsoFIGS. 5-8, showing perforatedbone interface side126 withperforations127.
• Central layer216, which is for example a solid titanium sheet, is placed withside202, and at leastperforated titanium sheet212 is placed with the opposite side ofcentral layer216, to form bone interface side210.Perforations214 ofsheet212 are larger thanperforations208, to reduce flow restriction on the core interface side.
• The bone interface side, barrier layer and core interface side (e.g.,side202,central layer216 and side210) are diffusion bonded together, instep808. If shaping is required (decision810), endplates (e.g.,endplates102 and106) are shaped from the bone interface side/barrier layer/core interface side assembly, instep812, and optionally coated with hydroxyapatite on their bone interface sides, in step814. Step814 is illustrated as a dotted box to indicate that hydroxyapatite coating may take place at other points inmethod700, for example atposition826 or elsewhere.
• The endplates are placed in a mold with their bone interface sides facing a core cavity, instep816, and core material is injection molded between the endplates, and allowed to extrude into the pores (e.g., mesh openings) in the core interface side, instep818. After setting (Step820), the interbody device is removed from the mold, instep822, and endplate and/or core features are created, inoptional step824. Bone interface sides are coated with hydroxyapatite instep826, if not already coated, or if additional coating is desired. Steps816-826 are similar to steps716-726, described in greater detail above.
• FIG. 33 shows a further method for forming an interbody device, such asdevice300. A porous core interface layer is placed on the back side of a featured titanium sheet, instep902, and the two are diffusion bonded together, instep904.
• In one example of steps902-904,porous sheet212 is placed oncore interface side328 ofmaterial forming endplate302 or306 (FIG. 24), and the porous sheet is diffusion-bonded with the material forming the endplate. Steps902-904 provide for an endplate having a plurality of machined webs, ridges (e.g., ridges313) or other surface-area increasing features for enhancing bone contact on the bone interface side, and pores on the core interface side for enhancing bonding with the core.
• Endplates are shaped from the diffusion bonded assembly if necessary (decision906), instep908. Bone interface sides are optionally coated with hydroxyapatite, instep910, and the endplates are placed in a mold with their core interface layers/sides facing a central cavity, instep912.
• Core material is injection molded between the endplates, and allowed to extrude into the pores (e.g., mesh openings) in the core interface side, instep914. After setting (Step916), the interbody device is removed from the mold, instep918, and endplate and/or core features are created, inoptional step920. Bone interface sides are coated with hydroxyapatite, in step922, if not already coated, or if additional coating is desired. Steps906-922 are similar to steps712-726, described in greater detail above.
• FIG. 34 shows acomposite interbody device1000 including asuperior endplate1002 and aninferior endplate1006, flanking acore1004.FIG. 35 is a simplified front view of assembleddevice1000.FIGS. 36-39 show details ofendplate1002 ofdevice1000, prior to formation of threading onendplate1002.FIGS. 34-39 are best viewed together with the following description.
• Core1004 is for example a PEEK core (i.e., injection molded thermosetting PEEK plastic) having one or more features1008, such as channels throughcore1004, for encouraging bone growth therethrough. Because PEEK is radiolucent,core1004 may include one ormore radio markers1014 for facilitating visualization ofcore1004 on x-ray, during or after implantation.Core1004 may alternately be made of any other biocompatible material that is sufficiently malleable for forming in a desired shape, yet strong enough to meet durability requirements of an intended implant site.Radiomarkers1014 may not be required wherecore1004 is made of a radio-opaque material.
• Features1008 may be machined aftercore1004 is injection molded, or features1008 may be extruded or otherwise formed withcore1004.Feature1008A is shown with respect toFIG. 40, and described below.Feature1008B is a horizontally-oriented channel that runs front-to-back throughcore104.Features1008C-1008E are horizontally-oriented, lateral openings intocore1004, or alternately, lateral channels that run throughcore1004, generally perpendicular to channel1008B and intersectingchannel1008B withincore1004.Channel1008B accommodates an insertion tool, such as a surgical drill, to facilitate placement ofdevice1000 at an implant site.Channel1008B may also allow bone growth throughdevice1000, whendevice1000 is implanted (e.g., between vertebrae to enhance spinal fusion, or at a hip socket to enhance hip fusion). For example, bone growing intodevice100 via a vertically-orientedslot1008A through device1000 (seeFIG. 40 and its description, below) may extend throughchannel1008B.
• Features1008C-E accommodate fusion-enhancers such as glues, bone graft or other fusion enhancing materials, and/or permit bone growth therethrough. For example, bone growing withinchannel1008A may branch intofeatures1008C-E, where not fully filled with a fusion-enhancer. When implanted between adjacent vertebrae, features1008B-E run generally perpendicular with a long axis of the spine.
• As shown,device1000 has a cylindrical shape with a relatively consistent diameter. Diameter d ofdevice1000 is for example about 20 mm. However, it will be appreciated that the diameter ofdevice1000 may vary from end to end, to facilitate insertion into a desired implant site. For example, where implanted in an intervertebral space,device1000 may taper from an end1007 distal to the spinal column, to an insertion end1005 that is proximal to the spinal column whendevice1000 is implanted.Endplates1002/1006 (and optionally,core1004, seeFIGS. 36-37) are threaded, to facilitate screwingdevice1000 into an implant site. For example,device1000 may be rotationally advanced into a cavity left by a surgical drill, the cavity having a diameter slightly smaller than diameter d. In one aspect,device1000 is self tapping. Asdevice1000 is screwed into place, for example into a cavity created between adjacent vertebrae,threads1015 decorticate bone of the vertebral endplates and provide bleeding bone edges to enhance bone growth onto and intodevice1000.Threads1015 may further allow for controlled widening of a collapsed disk space, to relieve pressure on compressed nerve roots. In addition,threads1015 increase surface area ofbone interface sides1026 ofendplates1002 and1006, for enhanced bone-to-device contact and bonding.
• In one aspect,endplates1002/1006 are threaded titanium, coated with hydroxyapatite (HA) to encourage both bone on-growth. It will be appreciated that other biocompatible metals such as molybdenum, cobalt-chrome, stainless steels and other biocompatible alloys, may be used in place of or in addition to titanium in formingendplates1002 and1006.Pores1027 penetratebone interface sides1026 ofendplates1002 and1006, providing a plurality of spaces for bone growth intoendplates1002 and1006.Core interface sides1028 ofendplates1002 and1006 are shown as non-porous surfaces, preventingcore1004 material from seeping intopores1026 during bonding ofcore1004 withendplates1002 and1006. However, it will be appreciated that an endplate configuration with porous bone interface and core interface sides, with a barrier layer therebetween, may be incorporated into one or both ofendplates1002 and1006. Such a configuration is described above with respect to endplate assembly200 (illustrated inFIGS. 19-22).
• Core1004 may be injection molded betweenendplates1002 and1006 in a manner similar to that described above (see, e.g.,FIG. 29 and the corresponding description).Endplates1002 and1006 may be formed withthreads1015 prior to injection-molding ofcore1004 between the endplates. Optionally,endplates1002 and1006 are formed as non-threaded, curved metallic sheets withpores1027 penetrating bone interface sides1026. See, e.g.,FIGS. 36-39, showing a non-threadedsuperior endplate1002. In one aspect,threads1015 and any additional features (such as features1008 and endplate apertures, shown and described with respect toFIGS. 40, 41 and 43) are machined intodevice1000 after injection molding and hardening ofcore1004 betweenendplates1002 and1006.
• Endplate1002 has a length (l_E1002) of about 30 mm and a width (w_E1002) of about 17-18 mm (seeFIG. 38). In one aspect, the length ofdevice1000 is also about 30 mm.Endplate1002 spans the length ofdevice1000. As shown inFIG. 37, the radius (r) ofdevice1000 is about 10 mm, whereas a distance (r₂) from the center (c) ofcore1004 tocore interface surface1028 ofendplate1002 is about 8.5 mm.Endplate1002 thus has an endplate height (h_E1002) of about 1.5 mm. Bottom edges ofendplate1002 are spaced at a distance x of about 5 mm from center c ofcore1004.Pores1027 have a major dimension (shown as pore width w_P1027) of about 600 microns.Endplate1002 andendplate1006 may be coated with hydroxyapatite before or after assembly withcore1004. In one example,endplates1002/1006 are formed by diffusion bonding any metallic components (i.e., a sheet formingcore interface side1028, a sheet formingbone interface side1026 and any barrier layer therebetween) together in a press shaped to produce a desired endplate shape or contour.Formed endplates1002/1006 are spray coated with hydroxyapatite prior to placement in a mold, andcore1004 is injection molded into a cavity betweenendplates1002/1006.
• FIGS. 40-44show device1000 with threading1015 applied tocore1004 andendplates1002,1006.FIGS. 40-44 are best viewed together with the following description. In one embodiment,core1004 is injection-molded between un-threaded superior andinferior endplates1002 and1006 (see, e.g.,superior endplate1002 as shown inFIG. 36), and threading1015 is thereafter machined onto the outer, middle surface ofcylindrical device1000. Thus, as shown inFIGS. 40-44,superior endplate1002,core1004 andinferior endplate1006 all include threading1015.Threading1015 may be continuously applied overcore1004 andendplates1002/1006, as shown inFIG. 40, eliminating the need to align threading1015 on previously-machinedendplates1002,1006 with threading ofcore1004.
• In one aspect,channel1008A is machined through the diameter ofcore1004 and aligns superior andinferior endplate apertures1010 and1012, respectively.Channel1008A is for example a narrow slot that opens into and runs substantially perpendicular to channel1008B throughcore1004, and likewise runs substantially perpendicular to, and may intersect one or more of,lateral channels1008C-1008E withincore1004.Superior aperture1010,channel1008A andinferior aperture1012 may be machined throughsuperior endplate1002,core1004 andinferior endplate1006 in a single operation to create an opening for bone growth entirely throughdevice1000. Optionally,endplates1002 and1006 are formed withrespective apertures1010 and1012 prior to placement in a mold, andchannel1008A is formed via molding. Bone growing intodevice1000 throughchannel1008A (viaendplate apertures1010,1012) may spread intochannel1008B and portions ofchannels1008C-E that are not blocked by fusion enhancing glue.
• Endplates1002 and1006 are curved to conform to a desired shape (e.g., a cylindrical shape) ofcore1004 and to facilitate screw-type insertion at an implant site.Device1000 length (l_D1000), shown inFIGS. 42-43, is about 30 mm.Channel1008A length (l_ch) and width (w_ch) are about 22 mm and 6 mm, respectively.Lateral channels1008C-1008E have a width (w_lat) and a length (l_lat) of about 4 mm. As previously noted, diameter d ofdevice1000 may be about 20 mm consistently, or may vary alongdevice1000, for example ifdevice1000 tapers from end1007 to end1005.
• It will be appreciated that althoughdevice1000 is shown and described with one superior and one inferior endplate,device100 may alternately include a plurality of endplates formed from titanium segments spaced about the perimeter ofdevice1000, and oriented along the long axis thereof.
• FIGS. 45-52 illustrate a generally kidney-shapedcomposite interbody device2000 having superior andinferior endplates2002 and2006, respectively, on inferior and superior sides of acore2004.Core2004 is made of a biocompatible material that is sufficiently malleable for forming in a desired shape, yet strong enough to meet durability requirements of an intended implant site. In one embodiment,core2004 is for example PEEK plastic that is injected betweenendplates2002 and2006 in a mold, and cooled to harden and bond. Alternately, superior andinferior endplates2002 and2006 may be press-fit withcore2004, bonded tocore2004 with a biocompatible adhesive, or mechanically attached tocore2004 using lock-and-key features such as v-grooves, or fasteners such as small screws.
• On aninsertion side2005,core2004 curves outward to form a nose portion2022 (seeFIG. 46).Nose portion2022 may facilitate insertion at an implant site (i.e., between adjacent vertebrae).Core2004 has one or more features2008, such as apertures into or channels throughcore2004, for encouraging bone through growth.Feature2008A is a vertically-oriented channel throughcore1004.Feature2008B is an aperture through aback side2007 of core2004 (side2007 is distal to the spinal cord when inserted between vertebrae), which facilitates insertion ofdevice2000 into an implant site.Aperture2008B is for example sized to accommodate a selected insertion tool. One or more of features2008 may optionally be packed with bone and/or other materials to enhance fusion.
• Aperture2008B opens intochannel2008A. Three insertion-side apertures2008C-20008E throughinsertion side2005 also open intochannel2008A.Features2008C-2008E may be filled partially or completely with fusion-enhancing glue or other fusion aids. Optionally or additionally, features2008C-E, and/or feature2008B, facilitate bone growth throughcore2004/device2000. For example, bone growing throughvertical channel2008A throughdevice2000 may encroach intofeatures2008B-E from withincore2004, where these features are not fully obstructed by a fusion aid.Features2008A-D may be machined aftercore2004 is molded (e.g., after injection-molding core2004 betweenendplates2002 and2006), or features2008A-2008D may be extruded or otherwise formed.
• As illustrated in the exploded view ofFIG. 47,channel2008A aligns with anaperture2010 insuperior endplate2002 and with anaperture2012 ininferior endplate2006 whendevice2000 is assembled as shown inFIGS. 45 and 46. Wherecore2004 is formed of radiolucent material, such as PEEK plastic, one ormore radio markers2014 facilitate visualization ofcore2004 on x-ray, for example oncedevice2000 is implanted.Superior endplate2002 bonds with a superiorendplate contact surface2016 ofcore304, andendplate2006 bonds with an inferiorendplate contact surface2018, as shown inFIG. 47.
• As also illustrated inFIG. 47,endplates2002 and2006 include a porous bone-interface side2026 and a porouscore interface side2028, separated by abarrier layer2216, which is for example similar tobarrier layer216 ofendplate assembly200. Porous metal sheets forming bone andcore interface sides2026 and2028 may be diffusion bonded withbarrier layer2216 therebetween, in a press shaped to lend any desired contour toendplate2002 and/or2026.Pores2027 ofbone interface side2026 are smaller thanpores2214 ofcore interface side2028. Larger pores2214 admitmolten core2004 material and facilitate core-to-endplate bonding, whilebarrier layer2216 prevents extrusion ofcore2004 material intosmaller pores2027, which are reserved for bone in-growth.Pores2027 may be sized for optimal bone in-growth; for example about 600 microns in diameter or across a major dimension.
• Alternately or additionally, as described above with respect toFIG. 25 anddevice300,endplates2002 and2006 may be machined with geometric features protruding therefrom to increase relative endplate surface area for bone on-growth on bone interface sides2026.Endplates2002 and2006 may be also be formed with ridges similar toridges313 of device300 (seeFIGS. 23-27), thin webs or other geometric features, for example features resulting from plate fracture, to increase endplate surface area.Core interface sides2028 ofendplates2002 and2006 may also bear geometric features for increasing surface area ofcore interface sides2028, to enhance bonding withcore2004 material. It will be appreciated thatendplates2002 and2004 may alternately be formed by metallic mesh layers separated by a barrier layer (as described above with respect to assembly200), or by bonding a porous metallic layer with a titanium sheet having ridges or other area-enhancing features on its opposite side (as described above with respect to device3000).
• FIG. 48 is view ofdevice2000 frominsertion side2005, andFIG. 49 is a cross-sectional view along line49-49 ofFIG. 48.FIGS. 48 and 49show feature2008D substantially aligned withfeature2008B, providing a horizontally oriented (whendevice2000 is implanted) channel completely throughdevice2000.Features2008D and2008B may be equal in size, as shown, or feature2008D may be smaller thanfeature2008B so that a surgical tool inserted throughfeature2008B will not fit completely intofeature2008D. In such a case, feature2008B provides support for an insertion device whileinsertion side2005,proximate feature2008D, provides resistance necessary to advancedevice2000 within an implant site.
• FIG. 50 is a bone-interface side2026 view of eithersuperior endplate2002 orinferior endplate2006, showing additional detail of bone interface pores2027. As shown, pores2027 need not be circular but may instead be square or rectangular (e.g., where formed by a metallic mesh). Other pore geometries are also within the scope hereof.
• FIG. 51 is an end view ofdevice2000, showingfeature2008C visible throughfeature2008E.Device2000 width (w_D2000), shown inFIG. 51 (a rear-side2007 view of device2000), may be similar to width w_Dofdevice100.Device2000 length (4D2000) and height (h_D2000), shown inFIG. 52, may also be similar to length (l_D) and height (h_D) of device100 (seeFIGS. 2-3). In one embodiment, l_D2000is 20-30 mm and h_D2000is about 8-15 mm.
• It will be appreciated thatdevice1000 ordevice2000 may be formed according to the methods illustrated inFIGS. 29-33. In one alternate example of method500 (FIG. 29), inferior andsuperior endplates1002 and1006 are assembled, instep502, and placed in a mold withcore interface sides1028 facing a core cavity in the mold, instep504.Core material1004 is injection molded into the cavity and, through the cavity, into pores of the core interface side, instep506. Note that while core interface pores are not shown with respect todevice1000, they are within the scope hereof.
• The endplate1002-core1004-endplate1006 assembly is allowed to set (for example, the assembly may be cooled untilcore1004 fully hardens), instep508, and removed from the mold, instep510. One or more offeatures1008A-1008E are formed ininterbody device1000, instep512. In one example ofstep512, features1008A-1008E incore1004 andapertures1010 and1012 throughrespective endplates1002 and1006 are formed indevice1000. For example, one channel may be drilled throughdevice1000 to formaperture1010,channel1008A and aperture1012 (SeeFIGS. 40-41). Bone interface surfaces of the device (i.e.,bone interface surfaces1026 ofendplates1002 and1006) are coated with hydroxyapatite, instep514. It will be appreciated that although shown as a final step inFIG. 29, hydroxyapatite may alternately or additionally be coated ontobone interface surfaces1026 prior to their incorporation intoendplates1002 and1006 (i.e., whereendplates1002 and1006 are formed in a multi-step process, as withassembly200,FIG. 19), or after formation ofendplates1002 and1006 and prior to placement in the mold.
• In one alternate example of method31, metallic wire mesh is selectively layered to formbone interface side2026, instep702. For example, one or more sheets of titanium wire mesh is placed or layered to formbone interface side2026 ofendplate2002 and/orendplate2006.Central barrier layer2216 is formed from a solid metallic (e.g., titanium) sheet placed onbone interface side2026, andcore interface side2028 is formed from larger-weave metallic mesh, placed oncentral barrier layer2216, insteps704 and706. In one aspect,bone interface side2026 is formed by selectively placing together titanium wire mesh layers204 and206 of assembly200 (FIG. 19), such thatbone interface pores2027 formed by openings in the mesh are at a desired orientation, one layer relative to the other. As noted above, pores2214 ofcore interface side2028 are larger thanpores2027 ofbone interface side2026, to reduce flow restriction on the core interface side for enhanced core-to-endplate bonding.
• Bone interface side2026,barrier layer2216 andcore interface side2028 are diffusion bonded together, in step708. If shaping is required (decision710),endplates2002 and2006) are shaped from the bone interface side/barrier layer/core interface side assembly, instep712, and optionally coated with hydroxyapatite onbone interface sides2026, in step714. Step714 is illustrated as a dotted box to indicate that hydroxyapatite coating may take place at other points inmethod700, for example atposition726 or elsewhere.
• Endplates2002 and2006 are placed in a mold withbone interface sides2026 facing a core cavity, instep716, andcore material2004 is injection molded between the endplates, and allowed to extrude intopores2027, instep718. After setting (step720),interbody device2000 is removed from the mold, instep722, andendplate2002/2006 and/orcore2004 features are created, inoptional step724. For example, afterrough interbody device2000 is removed from the mold,endplate apertures2010 and2012 are formed inendplates2002 and2006, respectively, if not already formed; andchannel2008A and any offeatures2008B-2008E that were not formed in molding are machined intocore2004. For example,apertures2010,2012 andchannel2008A are drilled throughdevice2000.
• Bone interface sides2026 may be coated with hydroxyapatite afterdevice2000 is machined with its desired features, afterendplates2002 and2006 are shaped from the bone interface side/barrier layer/core interface side assembly, or both. Alternately, the one or more mesh or perforated layers formingbone interface sides2026 may be coated with hydroxyapatite prior to placing the layers together to formbone interface sides2026, orbone interface side2026 may be coated with hydroxyapatite prior to its placement with central barrier layer2116. The depth and placement of hydroxyapatite coating may vary as a function of an intended implant site.
• While the present invention has been described above, it should be clear that many changes and modifications may be made to the process and product without departing from the spirit and scope of this invention. For example, select or all components of the above-described devices may provide an inter-bone bridge used for bone fusions outside of the spine. Additionally, components of different endplates described above may be combined, without departing from the scope hereof.

Claims (20)

What is claimed is:

1. A composite threaded interbody device, comprising:

an outer surface that is cylindrical or conical;

a plastic core having two outer sections, each of the outer sections forming a respective portion of the outer surface and spanning a respective azimuthal range in an azimuthal dimension relative to a longitudinal axis of the outer surface, the outer sections being separated from each other in the azimuthal dimension by two recessed sections that are recessed from the outer surface; and

two threaded endplates coupled to the two recessed sections and spanning gaps between the outer sections, to complete the outer surface.

2. The composite threaded interbody device ofclaim 1, each of the outer sections being threaded.

3. The composite threaded interbody device ofclaim 2, threads of the outer sections cooperating with threads of the threaded endplates to form a common thread of the outer surface, the common thread spiraling about the longitudinal axis.

4. The composite threaded interbody device ofclaim 3, the common thread being interrupted by one or more channels passing through the composite threaded interbody device.

5. The composite threaded interbody device ofclaim 1, diameter of the outer surface being uniform along the longitudinal axis such that the threaded outer surface is cylindrical.

6. The composite threaded interbody device ofclaim 1, diameter of the outer surface decreasing along the longitudinal axis from a first end of the composite interbody device to a second end of the composite interbody device, such that the threaded outer surface is conical.

7. The composite threaded interbody device ofclaim 1, the plastic core forming at least one channel allowing bone growth therethrough.

8. The composite threaded interbody device ofclaim 7, the at least one channel further including a plurality of lateral channels, each of the lateral channels passing through each of the outer sections.

9. The composite threaded interbody device ofclaim 8, the at least one channel further including a slot passing through each of the threaded endplates, the slot intersecting the lateral channels.

10. The composite threaded interbody device ofclaim 7, the plastic core further forming a longitudinal channel spanning length of the plastic core along the longitudinal axis.

11. The composite threaded interbody device ofclaim 1, each of the endplates being made of metal.

12. The composite threaded interbody device ofclaim 11, each of the endplates being coated with hydroxyapatite.

13. The composite threaded interbody device ofclaim 1, length of the outer surface along the longitudinal axis exceeding diameter of the outer surface.

14. A method for manufacturing a composite threaded interbody device, comprising:

coupling two endplates in two respective recessed sections of a plastic core such that the endplates cooperate with outer sections of the plastic core, from which the recessed sections are recessed, to form an outer surface of the composite threaded interbody device, the outer surface being cylindrical or conical, the outer sections being separated from each other in an azimuthal dimension, relative to a longitudinal axis of the outer surface, by the recessed sections; and

after the step of coupling, forming, in the endplates and the outer sections, a common thread that spirals about the longitudinal axis.

15. The method ofclaim 14, further comprising, after the step of coupling, forming at least one channel passing through the composite threaded interbody device between and through the outer sections.

16. The method ofclaim 14, further comprising coating the endplates with hydroxyapatite.

17. A method for manufacturing a composite threaded interbody device, comprising:

coupling two threaded endplates in two respective recessed sections of a plastic core such that the endplates cooperate with outer sections of the plastic core, from which the recessed sections are recessed, to form an outer surface of the composite threaded interbody device, the outer surface being cylindrical or conical, the outer sections being separated from each other in an azimuthal dimension, relative to a longitudinal axis of the outer surface, by the recessed sections.

18. The method ofclaim 17, further comprising, after the step of coupling, forming at least one channel passing through the composite threaded interbody device between and through the outer sections.

19. The method ofclaim 18, further comprising coating the endplates with hydroxyapatite.

20. The method ofclaim 17, further comprising aligning threads of the threaded endplates with threads of the outer sections to form a common thread spiraling about the longitudinal axis.

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