Composite vertebral spacers and instrument
11020237 · 2021-06-01
Assignee
Inventors
Cpc classification
A61F2002/2835
HUMAN NECESSITIES
A61F2002/30772
HUMAN NECESSITIES
A61F2002/2817
HUMAN NECESSITIES
A61F2002/30062
HUMAN NECESSITIES
A61F2002/30841
HUMAN NECESSITIES
A61F2230/0028
HUMAN NECESSITIES
A61F2002/30131
HUMAN NECESSITIES
A61F2220/0041
HUMAN NECESSITIES
A61F2002/30471
HUMAN NECESSITIES
A61F2220/0091
HUMAN NECESSITIES
A61F2002/4627
HUMAN NECESSITIES
A61F2/447
HUMAN NECESSITIES
A61F2002/30579
HUMAN NECESSITIES
A61F2002/30433
HUMAN NECESSITIES
A61F2/4455
HUMAN NECESSITIES
A61F2230/0013
HUMAN NECESSITIES
International classification
Abstract
An intervertebral fusion cage that is adapted to contain an inserter within its inner volume during insertion of the cage.
Claims
1. An intervertebral fusion cage, comprising: a leading portion having a front surface and a back surface spaced from the front surface in a backward direction, the back surface being adapted for reception of a rod, wherein the leading portion defines a first pivot hole that extends therein; and first and second support members that extend backwards from the leading portion and terminating at respective back surfaces, each member having respective upper and lower surfaces adapted for bearing against and griping adjacent vertebral bodies, wherein the first support member defines a second pivot hole, wherein each of the first and second support members are pivotally connected to the leading portion, and a pivot pin extends into the first and second pivot holes so as to pivotally attach the first support member to the leading portion, wherein the pivot pin is oriented along a direction that separates the respective upper surfaces from the respective lower surfaces, wherein the intervertebral fusion cage is responsive to movement of the rod in the backward direction such that the intervertebral fusion cage moves from an initial position to a fully expanded position whereby 1) the back surface of the first support member moves away from the back surface of the second support member, and 2) no portion of either of the first and second support members is spaced from the leading portion in a forward direction that is opposite the backward direction, and wherein the intervertebral fusion cage is configured such that movement of the rod in the backward direction causes a force in the backward direction to be applied to the leading portion.
2. The intervertebral fusion cage of claim 1, wherein when the fusion cage is in the initial position the back surfaces of the first and second support members are aligned with each other along a first straight line, and the leading portion is closer to the first straight line in the backward direction when the fusion cage is in the fully expanded position as compared to when the fusion cage is in the initial position.
3. The intervertebral fusion cage of claim 2, wherein the front surface of the leading portion is curved along a convex path.
4. The intervertebral fusion cage of claim 3, comprising a recess that extends into the leading portion in a forward direction opposite the backward direction, wherein the recess is configured to receive the rod so as to couple the rod to the intervertebral fusion cage.
5. The intervertebral fusion cage of claim 4, wherein the recess is threaded so as to threadedly couple to the rod.
6. An intervertebral fusion system comprising: the intervertebral fusion cage of claim 4; and the rod.
7. The intervertebral fusion cage of claim 2, wherein the respective upper and lower surfaces are spaced from each other along a first direction that is perpendicular to the backward direction, and the pivot pin is oriented along the first direction.
8. The intervertebral fusion cage of claim 2, wherein the first and second support members extend parallel to each other when the fusion cage is in the initial position.
9. The intervertebral fusion cage of claim 8, wherein the first support member flares away from the second support member as the first support member extends in the backward direction when the fusion cage is in the fully expanded position.
10. The intervertebral fusion cage of claim 2, wherein the first and second support members comprise teeth at their respective upper and lower surfaces.
11. The intervertebral fusion cage of claim 2, further comprising first and second members that bear against the back surfaces of the first and second support members, respectively, as the cage moves from the initial position to the fully expanded position.
Description
DESCRIPTION OF THE FIGURES
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DETAILED DESCRIPTION OF THE INVENTION
(23) The present invention relates to a spinal interbody spacer that is easy to insert, fracture resistant, migration resistant, and Tillable with a flowable biologic material after insertion.
(24) Now referring to
(25) Upon each of the upper and lower surfaces of the cage, there is provided a plurality of teeth 21. When the cage is inserted and the inserter is removed, these teeth bite into the adjacent vertebral bodies and thereby resist migration of the cage.
(26) Each of the support members further comprises a side surface 23 extending between its upper and lower surfaces, each side surface having at least one transverse hole 25 therethrough. The transverse hole allows bone growth therethrough, thereby further securing the cage within the intervertebral space.
(27) In some embodiments, the front surface of the leading end of the cage is tapered. This tapered nose 27 can distract the disc space during its insertion into the disc space, thereby providing for ease of insertion.
(28) Also shown in
(29) In other embodiments, the back surface of the leading end forms a threaded recess for threadable reception of a rod.
(30) As shown, the ends of the leading end and the support members are integrally connected.
(31) In preferred embodiments, the back surfaces of the support members of the cage are used as stabilizers whereby a forward force upon these back surfaces carefully counterbalances the backward force used to withdraw the rod from the cage. This forward force keeps the cage in the disc space during withdrawal of the rod. Preferably then, the back surfaces are configured to stably receive the laterally-spaced extensions that extend from the distal face of the cannula and provide the biasing forward force. In some embodiments thereof, the back surface of each support member has a concave recess providing such stability. However, in other embodiments, the back surface of each support member may be flat.
(32) In use, the “U” shaped implant of
(33) Therefore, in accordance with the present invention, there is provided an assembly comprising: a) an intervertebral fusion cage having an interior space, and b) a rod adapted to insert the cage into an intervertebral space, the rod having a distal end and an intermediate portion,
wherein the distal end of the rod is connected to the cage, and
wherein the intermediate portion of the rod is housed within the interior space of the cage.
(34) Also in accordance with the present invention, there is provided a method of inserting a fusion cage, comprising the steps of: a) providing an intervertebral fusion cage having a leading end having a back surface and a trailing end, b) coupling a distal end of an inserter having a slidable rod therein to the back surface of the leading end of the cage, c) inserting the cage into an intervertebral space, d) withdrawing the rod from the cage.
(35) Now referring to
(36) Preferably, as shown, the leading end has an arcuate shape. Also preferably, the leading end has a beveled nose 77 defined by converging upper and lower surfaces. This beveled nose facilitates cage insertion.
(37) Preferably, the upper and lower surfaces of the support members are adapted for gripping the opposing vertebral endplates. Preferably, these surfaces contain outwardly extending teeth 79 that provide stability to the cage.
(38) Preferably, each support member has a throughhole 80 extending therethrough and each cross-member has a throughhole 81 extending therethrough. The cross members provide for substantial containment of the injectable bone graft paste and add stiffness to the construct. These holes are adapted for encouraging bone growth therethrough.
(39) As shown, the cage preferably has a substantially rectangular cross-section.
(40) In this embodiment, an inserter rod can anchor into the back surface of the leading end of the cage.
(41) Therefore, in accordance with the present invention, there is provided an intervertebral fusion cage, comprising: a) a leading end having a right and left ends, a front surface and a back surface, b) first and second support members extending backwards from the right and left ends and terminating in a respective back surface, each member having an upper and lower surface adapted for bearing against and gripping adjacent vertebral bodies, c) an open trailing end formed by the back surfaces of the support members, and d) a strut connecting the first and second support members, the strut being located between the leading end and the open trailing end of the cage, the strut having a back surface being adapted for reception of an inserter rod.
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(43) The cage is the cage shown in
(44) The inserter of
(45) Therefore, in accordance with the present invention, there is provided an apparatus for inserting a fusion cage having a leading end and a trailing end, comprising: a) a cannula having a bore therethrough, a distal end face and at least two extensions extending distally from the distal end face, each extensions having a distal end adapted for bearing against the trailing end of the cage, and b) a rod slidably received within the bore of the cannula, the rod having a distal end adapted for bearing against the leading end of the cage.
(46) Also in accordance with the present invention, there is provided an assembly comprising: a) an intervertebral fusion cage having a leading end and a trailing end, and b) an inserter comprising: i) a cannula having a bore therethrough, a distal end face and at least two extensions extending distally from the distal end face, each extension having a distal end bearing against the trailing end of the cage, and ii) a rod slidably received within the bore of the cannula, the rod having a distal end bearing against the leading end of the cage
(47) Lastly,
(48) In use, the assembly of
(49) Now referring to
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(51) The assembled version of
(52) It has further been appreciated that if only the threaded inner rod is removed, then there exists a channel in the insertion instrument through which injectable bone graft material can be injected.
(53) Now referring to
(54)
(55) The assembled version of
(56) In some embodiments, hinges are provided between each end of the leading portion of the cage and each of the support members. These hinges allow the cage to be spread after insertion in order to increase the effective surface area (i.e., footprint) covered by the implant. Increasing the footprint beneficially improves the stability of the construct.
(57) Now referring to
(58) Therefore, in accordance with the present invention, there is provided an intervertebral fusion cage, comprising: a) a leading portion having a first and second ends extending backwards, a front surface and a back surface, an upper surface and a lower surface, and a pivot hole provided in each of the ends which extends from the upper surface to the lower surface, b) first and second support members, each support member having: i. an upper and lower surface adapted for bearing against and gripping adjacent vertebral bodies, ii. a back surface, the back surfaces forming an open trailing end therebetween, iii. a front end having a pivot hole which extends from the upper surface of the support member to the lower surface of the support member, and c) first and second pivot pins respectfully provided in the pivot holes to pivotally connect each end of the leading end and the front end of each support member.
(59) Each support member has a bump 245 extending medially from its inside surface 247. As will be explained later in more detail, these bumps facilitate the splaying of the support members to increase the footprint of the cage.
(60) The insertion instrument of the present invention comprises three components; a) a centrally-disposed cylindrical rod 251, b) a pair of laterally disposed cage holders 253, and c) upper 255 and lower 257 rails.
(61) The cylindrical rod is adapted to fit within the open recess formed between the two support members. The rod comprises an enlarged head 259 having an annular recess 261 therebehind, a distal threaded portion 263 and an intermediate portion 265. The annular recess corresponds in shape and dimension to the bumps 245 situated on the inside surfaces of the support members. The distal threaded portion is adapted to be threadably received in the recess of the C-shaped leading portion of the cage, thereby securing the instrument to the cage. The intermediate portion of the rod is housed within the interior space of the cage.
(62) In use, after cage insertion, the threaded portion is unthreaded to free the rod for proximal movement in respect of the cage. When the head of the cylindrical rod is moved backward so as to be removed from the cage, the hinged support members are forced to pivot outwards to increase the footprint of the cage. The closer these bumps are situated to the arcuate leading end of the cage, the greater the splay of the support members. The cylindrical rod is the first instrument component to be removed from the disc space.
(63) The front ends 267 of the upper 255 and lower 257 rails are adapted to fit within the upper and lower grooves provided on the C-shaped leading portion of the cage, while the posterior portion of the rail is adapted to bear against the upper and lower surfaces of the cylindrical rod. Each rail has a thickness T that allows the rail to extend beyond the respective upper and lower surfaces of both the C-shaped leading portion and the support members of the cage. Further, the outer surfaces 271 of the rails are smooth. Because the smooth rails extend beyond the upper and lower surfaces of the cage, they provide a smooth insertion of the cage-instrument assembly into the disc space. For additional ease of insertion, the front end of each rail may be provided with a taper 272 that essentially extends from the taper of the front nose of the C-shaped leading portion of the cage. The rails are the second instrument component to be removed from the disc space.
(64) Therefore, in accordance with the present invention, there is provided an intervertebral fusion cage comprising, a) a leading end and a trailing end, b) first and second longitudinal support members extending between each end, each member having an upper and lower surface adapted for bearing against and gripping adjacent vertebral bodies, each upper and lower surface having a longitudinal groove therein, and c) a plurality of rails, each rail having a smooth outer surface and each rail received in a respective groove of the support member and extending out of the respective groove.
(65) The pair of laterally disposed cage holders are disposed upon each side of the cylindrical rod. Each cage holder has a front end 273 adapted to bear against the back surface of each support member portion of the cage. These front ends prevent the cage from moving back when the cylindrical rod and the rails are removed. The cage holders are the third and last instrument component to be removed from the disc space.
(66) Now referring to
(67) As seen in
(68) Now referring to
(69) As shown,
(70)
(71) In preferred embodiments, the cage of
(72) Now referring to
(73) The composite nature of this implant in conjunction with the mating condition of the inserter instrument will also allow for very forceful manipulation of the implant during insertion without damaging the implant. In essence, the PEEK laminates are not loaded by the insertion force.
(74) Since the pins 317 are mainly in compression between the inserter components, the inserter will carry the majority of the insertion load. To the extent the pins 317 carry any impaction force, the pins are advantageously made of a high strength, ductile metal such as titanium, and are preferably a titanium alloy, and so can bear such loads. The metallic nature of the pins allows for forceful manipulation of the assembly during insertion into the disc space. At the same time, selection of a somewhat flexible polymer such as PEEK for the material of construction of the laminate components avoids the stress shielding issues associated with purely titanium cage designs. Selection of the woven carbon fiber (as opposed to chopped carbon fiber) will enhance the strength of the PEEK composite.
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(76) In some embodiments, as in
(77) In some embodiments, the struts have additional side holes (not shown), wherein those side holes are not engaged by a cross-pin. The presence of these holes will enhance bone ingrowth through the struts.
(78) In some embodiments, the upper and lower surfaces of the struts have a plurality of fine teeth 325 extending therefrom to resist implant migration.
(79) Now referring to
(80) In some embodiments, the fusion cage includes smooth retractable rails positioned on the top and bottom of the cage. Now referring to
(81) As shown in
(82) In some embodiments, the rails are rigid. Such rigid rails may be conveniently used with substantially straight cages. In some embodiments, the rails are flexible. Such flexible rails may be conveniently used with curved cages such as banana cages.
(83) In some embodiments (not shown), the rail comprises an outer tube having a smooth outer surface and an inner rod. When assembled, the tube and rod have a height that allows the to extend outward past the upper and lower teeth of the cage. During insertion, the tube-rod assembly eases insertion load. When the cage has been inserted, the rod is withdrawn and the tube collapses under the force of the tensioning load of the functional spinal unit. Thus, the adjacent boney endplates of the patient collapse upon the cage, and the aggressive teeth of the cage will engage the bone and effectively prevent migration of the implant.
(84) In some embodiments (not shown), the rails can be molded onto the cage as a fast dissolving polymer. During insertion, the smooth rails ease insertion. Once the cage is set in place, the rails dissolve, thereby allowing the adjacent boney endplates of the patient to collapse upon the cage.
(85) In some embodiments, a single smooth cable may act as both an upper and lower rail by wrapping around an end of the cage. During insertion, the smooth rails ease insertion. At this time, tensioning of the cable may serve to hold the cage on the inserter.
(86) Once the cage is set in place, the surgeon pulls a single end of the cable in order to remove the whole cable from the cage. In some embodiments, the cable is coated with a smoothing polymer such as Teflon in order to reduce friction.
(87) The recognition that inserter designs can now occupy the interior volume of the cage has special application in the field of intervertebral fusion cages having a banana shape. In these banana cages, the cage can be made to attach to an inserter at the midpoint of the cage, which is the strongest portion of the cage.
(88) Now referring to
wherein the strut has a threaded recess opening 465 onto the trailing space for reception of a threaded distal end of an inserter and,
wherein the trailing side surface has a throughhole 467 therethrough for slidable reception of the inserter.
(89) Now referring to
(90) Typically, the inserter of the present invention can be made out of any material commonly used in medical instruments. If the inserter is designed to be reusable, then it is preferred that all of its components be made of stainless steel. If the device is designed to be disposable, then it is preferred that at least some of the components be made of plastic. Preferably, at least one component of the inserter is sterilized. More preferably, each component is sterilized.
(91) The intervertebral fusion cage of the present invention may be manufactured from any biocompatible material commonly used in interbody fusion procedures. In some embodiments, the cage is made from a composite comprising 40-99% polyarylethyl ketone PAEK, and 1-60% carbon fiber. Such a cage is radiolucent. Preferably, the polyarylethyl ketone PAEK is selected from the group consisting of polyetherether ketone PEEK, polyether ketone ketone PEKK, polyether ketone ether ketone ketone PEKEKK, and polyether ketone PEK. Preferably, cage is made from woven, long carbon fiber laminates. Preferably, the PAEK and carbon fiber are homogeneously mixed. Preferably, the composite consists essentially of PAEK and carbon fiber. Preferably, the composite comprises 60-80 wt % PAEK and 20-40 wt % carbon fiber, more preferably 65-75 wt % PAEK and 25-35 wt % carbon fiber. In some embodiments, the cage is made from materials used in carbon fibers cages marketed by DePuy Spine, Raynham, Mass., USA. In some embodiments, the composite is PEEK-OPTIMA™, available from Invibio of Greenville, N.C.
(92) In other embodiments, the cage is made from a metal such as titanium alloy, such as Ti-6Al-4. In other embodiments, the cage is made from an allograft material. In some embodiments, the cage is made from ceramic, preferably a ceramic that can be at least partially resorbed, such as HA or TCP. In other embodiments, the ceramic comprises an oxide such as either alumina or zirconia. In some embodiments, the cage is made from a polymer, preferably a polymer that can be at least partially resorbed, such as PLA or PLG.
(93) In preferred embodiments, the cage is provided in a sterile form.
(94) In summary, the cage implant of the present invention distracts the disc space during insertion. It is easy to insert and optimizes clinical performance once in place because it resists migration and subsidence, has an appropriate stiffness for load sharing, is preferably radiolucent and has a shape that is able to contain injected graft material such as growth factors. In addition, the cage is robust over a wide variation of surgical technique because it will not break even when large forces are applied thereto.
(95) The cage of the present invention is compatible with the broad use of injectable paste-like bone grafting materials, such as BMP-containing pastes because it is designed to be inserted empty and then filled with graft in-situ. With the availability of these injectable pastes, cages will no longer require large, contiguous internal volumes to accept morselized/granular bone graft. Spaces can be smaller and more numerous.
(96) The cage of the present invention allows an insertion instrument to occupy the internal volume of the cage so as to minimize the overall size of the inserted cage as well as to bear insertion loads. The inserter can also possess smooth upper and lower surfaces to reduce friction and thereby increase the ease of insertion. The cage of the present invention will not experience large loads during insertion.