Nubbed Plate
20210322180 · 2021-10-21
Inventors
- Nicholas Pavento (North Attleboro, MA, US)
- John Riley Hawkins (Cumberland, RI, US)
- Sheryl Furlan (Middleboro, MA, US)
- Douglas Raymond (Bridgewater, MA, US)
Cpc classification
A61F2002/30578
HUMAN NECESSITIES
A61F2310/00023
HUMAN NECESSITIES
A61F2002/30787
HUMAN NECESSITIES
A61F2002/2835
HUMAN NECESSITIES
A61F2310/00017
HUMAN NECESSITIES
A61F2002/2817
HUMAN NECESSITIES
A61F2002/30607
HUMAN NECESSITIES
A61F2310/00407
HUMAN NECESSITIES
A61F2/30744
HUMAN NECESSITIES
A61F2220/0008
HUMAN NECESSITIES
A61F2310/00029
HUMAN NECESSITIES
A61F2002/30622
HUMAN NECESSITIES
A61F2002/30594
HUMAN NECESSITIES
A61F2/447
HUMAN NECESSITIES
A61F2002/30616
HUMAN NECESSITIES
A61F2002/448
HUMAN NECESSITIES
A61F2/4455
HUMAN NECESSITIES
A61F2/4465
HUMAN NECESSITIES
A61F2310/00239
HUMAN NECESSITIES
A61F2/30965
HUMAN NECESSITIES
International classification
Abstract
A separate nub component between the plate and an intervertebral fusion cage, wherein the nub is attached to the plate. The nub lessens the undesired pivotal movement of the plate. It is believed that when the nub fits snugly between the endplates of the adjacent vertebral bodies, it acts as a stop against the undesired pivotal movement of the plate.
Claims
1. A method of implanting an intervertebral fusion device, the method comprising the steps of: inserting an elongated member into an intervertebral space; and moving a body about a component along a curved path, wherein the component is interposed between the body and the elongated member and separate from both the body and the elongated member.
2. An intervertebral fusion device comprising: an elongated member configured to be inserted into an intervertebral space; and a component; and a body movable about the component along a curved path, wherein the component is interposed between the body and the elongated member.
Description
DESCRIPTION OF THE FIGURES
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DETAILED DESCRIPTION OF THE INVENTION
[0037] Now referring to
[0038] a) an intervertebral fusion cage 1 having an anterior wall 3, a posterior wall 5, a leading wall 7 and a trailing wall 9 connecting the anterior and posterior walls to form a central vertical throughhole 11, an upper surface 13 adapted for gripping an upper endplate and a lower surface 15 adapted for gripping a lower endplate;
[0039] b) a bone plate 21 comprising an upper hole 23, a lower hole 25, and a central hole 27 disposed substantially between the first and second holes, [0040] c) a nub 31 interposed between the bone plate and the trailing wall of the cage, the nub comprising: [0041] i) a first wall 33 contacting the trailing wall of the cage, [0042] ii) a second wall 35 contacting the bone plate, [0043] iii) a threaded throughhole 37 extending from the first wall to the second wall, and
[0044] d) a threaded post 41 received in the throughhole of the nub and passing through the central hole of the bone plate.
[0045] In some embodiments, the assembly has a polyaxial joint. It is believed that the inclusion of this polyaxial joint is very advantageous to the performance of the device. It has been noticed that typical variations in human physiology often result in a situation in which the sidewalls of the adjacent vertebrae that hold the plate are not coplanar with each other. Rather, one sidewall often extends out farther than its adjacent sidewall. Thus, when a conventional cage-plate assembly (in which the plate is rigidly attached to the cage in a perpendicular relationship) is used on a typical functional spinal unit, the lack of a coplanar relationship in the vertebral sidewalls leads to a fixation situation in which only one of the vertebral sidewalls will actually contact the plate. This asymmetrical contact undesirably leads to stress concentration and poor distribution of biomechanical forces (as one screw is loaded more), leading to bony fracture.
[0046] It is believed that a polyaxial joint in the cage-plate assembly alleviates these concerns. When the cage-plate assembly of the present invention is used on a typical functional spinal unit lacking coplanar vertebral sidewalls, the plate can be polyaxially adjusted about the cage until it contacts each of the sidewalls and then locked at that desired angle. This produces a fixation in which asymmetrical contact is eliminated.
[0047] Therefore, in accordance with the present invention, there is provided an intervertebral fusion device comprising:
[0048] a) an intervertebral fusion cage having an anterior wall, a posterior wall, leading and trailing walls connecting the anterior and posterior walls to form a central vertical throughhole, an upper surface adapted for gripping an upper endplate and a lower surface adapted for gripping a lower endplate, the upper and lower surface defining a cage height;
[0049] b) a bone plate comprising a bone contacting surface, and outer surface, upper and lower holes passing from the bone-contacting surface to the outer surface, and a projection extending distally from the bone contacting surface and having a height,
[0050] wherein the bone plate is connected to the trailing wall of the cage via a polyaxial connection.
[0051] Also in accordance with the present invention, there is provided an assembly device for fusing a disc space, comprising:
[0052] a) a bone plate comprising a bone-contacting inner surface, an outer surface, upper and lower holes, a central hole, each hole passing from the outer surface to the inner surface,
[0053] b) an intervertebral component comprising: [0054] i) a first wall facing the disc space, [0055] ii) a second wall contacting the inner surface of the bone plate,
[0056] c) first and second bone anchors passing through the upper and lower holes of the bone plate, wherein the bone plate forms a polyaxial joint with the intervertebral component.
[0057] In a first polyaxial embodiment, and now referring to
[0058] Therefore, in accordance with the present invention, there is provided an interbody device for fusing a disc space, comprising:
[0059] a) a bone plate comprising a bone contacting inner surface, an outer surface, upper and lower holes, a central hole having a spherical surface thereon, each hole passing from the outer surface to the inner surface,
[0060] b) an intervertebral component comprising: [0061] i) a first wall facing the disc space, [0062] ii) a second wall contacting the inner surface of the bone plate, [0063] iii) a threaded throughhole extending from the first wall to the second wall,
[0064] c) first and second bone anchors passing through the upper and lower holes of the bone plate,
[0065] d) a post having a proximal spherical head and a distal threaded shaft,
[0066] wherein the inner surface of the bone plate contacts the second wall of the intervertebral component,
[0067] wherein the central hole of the bone plate and the threaded throughhole of the intervertebral component align,
[0068] wherein the distal threaded shaft of the post is threadably received in the threaded throughhole of the nub, and wherein the proximal spherical head of the post is received in the spherical surface of the central hole of the bone plate to form a polyaxial joint).
[0069] Now referring to
[0070] Likewise, in some embodiments in which the plate and post form a polyaxial joint, the inner surface of the bone plate has a concave surface 49. This concave surface is useful in the polyaxial joint embodiments in which the second wall of the nub is convex because it accommodates more tilting of the plate with respect to the nub while maintaining the joint.
[0071] In some embodiments, and now referring to
[0072] In a second polyaxial preferred embodiment, and now referring to
[0073] It is believed that the device of
[0074] Therefore, in accordance with the present invention, there is provided an interbody device for fusing a disc space, comprising:
[0075] a) a bone plate comprising a bone contacting inner surface, an outer surface, upper and lower holes, a central hole, each hole passing from the outer surface to the inner surface, and an annular projection extending distally from the inner surface about the central hole,
[0076] b) an intervertebral component comprising: [0077] i) a first wall facing the disc space, [0078] ii) a second wall contacting the inner surface of the bone plate, [0079] iii) a throughhole extending from the first wall to the second wall, iv) a recessed surface extending distally about the throughhole,
[0080] c) first and second bone anchors passing through the upper and lower holes of the bone plate,
[0081] wherein the annular projection of the bone plate forms a polyaxial joint with the recessed surface of the intervertebral component.
[0082] In general, the cage of the present invention can be any interbody fusion cage suitable for promoting fusion between two vertebral bodies. The cage can be adapted for lumbar, cervical or thoracic use. The cage can be adapted for lateral, posterior, or anterior insertion. In some preferred embodiments, the cage is adapted for lateral approach to the lumbar spine. Typically, the cage will have an anterior wall, a posterior wall, leading and trailing walls connecting the anterior and posterior walls to form a central vertical throughhole, an upper surface adapted for gripping an upper endplate and a lower surface adapted for gripping a lower endplate. The central vertical throughhole facilitates bone growth between the two adjacent vertebral endplates. Each of the posterior and anterior walls may have ventral-dorsal throughholes 62 therethrough in order to accommodate fusion as well. The leading wall of the lateral cage may have a bulleted nose 63 that eases insertion into the disc space.
[0083] The bone plate of the present invention typically comprises a bone-contacting inner surface, an outer surface, and upper and lower holes passing from the bone-contacting surface to the outer surface. Bone anchors pass through these upper and lower holes to thereby anchor the plate to the adjacent vertebral bodies.
[0084] In some embodiments, and now referring to
[0085] In some embodiments, the central hole in the plate is provided in the form of an elongated slot. The elongated slot allows for slidable adjustment of the plate upon the nub, thereby allowing for a fine tuning of the plate location after the nub location is set.
[0086] In some embodiments, the bone-contacting inner surface of the plate narrows distally. This contouring helps the plate fit between the adjacent vertebrae. This feature is believed to be advantageous in MIS procedures in which the components are inserted into the spinal area through a tube in the absence of a clear line of sight on the part of the surgeon.
[0087] In some embodiments, as in
[0088] In some embodiments, as in
[0089] In some embodiments, as in
[0090] As discussed above, the purpose of the nub is to prevent undesired pivoting of the plate about its centerpoint.
[0091] In some embodiments, the cage, plate and nub are present as separate components. This condition maximizes the surgeon's ability to adjust the location of the plate after fixing the locations of the cage and nub.
[0092] In some embodiments, and now referring to
[0093] Therefore, in accordance with the present invention, there is provided an intervertebral fusion device comprising:
[0094] a) an intervertebral fusion cage having an anterior wall, a posterior wall, leading and trailing walls connecting the anterior and posterior walls to form a central vertical throughhole, an upper surface adapted for gripping an upper endplate and a lower surface adapted for gripping a lower endplate,
[0095] b) a separate bone plate component comprising a bone contacting surface, and outer surface, upper and lower holes passing from the bone-contacting surface to the outer surface, and a projection extending distally from the bone contacting surface,
[0096] wherein the projection of the bone plate contacts the trailing wall of the cage. In some embodiments, and now referring to
[0099] wherein each of the upper and lower surfaces of the nub is disposed between the first and second walls of the nub.
[0100] In preferred embodiments, gripping is accomplished by providing a plurality of teeth 75 upon each of the upper and lower surfaces. The purpose of these nub teeth is to enhance the snug fit of the nub between the vertebral bodies and thereby further prevent the rocking of the plate.
[0101] In some embodiments, and now referring to
[0102] In some embodiments, the nub height is not less than the cage height. This condition enhances the snug fit of the nub between the vertebral bodies and thereby further prevent the rocking of the plate.
[0103] In some embodiments, the nub height is substantially the same as the cage height. This condition possess the attributes of the two conditions described above.
[0104] In some embodiments, and now referring to
[0105] The function of the post is to retain the plate on the nub. Typically, and now referring to
[0106] Typically, the post passes through the central hole of the plate and threads into the nub. However, in some embodiments, the post can thread into the cage as well.
[0107] Generally, and now referring to
[0108] Generally, and now referring to
[0109] The cages of the present invention may be made from any non-resorbable material appropriate for human surgical implantation, including but not limited to, surgically appropriate metals, and non-metallic materials, such as carbon fiber composites, polymers and ceramics.
[0110] The interbody devices are preferably made out of PEEK or CFRP or any other suitable material providing adequate strength and radiolucency. However, implantable metals such as titanium or stainless steel components may be required to ensure adequate strength for either the interbody device. In some cases the interbody device can be made as a combination of PEEK and metal. In some cases, resorbable materials such as polylactide, polyglycolide, and magnesium are preferred.
[0111] In some embodiments, the cage material is selected from the group consisting of PEEK, ceramic and metallic. The cage material is preferably selected from the group consisting of metal and composite (such as PEEK/carbon fiber).
[0112] If a metal is chosen as the material of construction for a component, then the metal is preferably selected from the group consisting of titanium, titanium alloys (such as Ti-6A1-4V), chrome alloys (such as CrCo or Cr—Co—Mo) and stainless steel.
[0113] If a polymer is chosen as a material of construction for a component, then the polymer is preferably selected from the group consisting of polyesters, (particularly aromatic esters such as polyalkylene terephthalates, polyamides; polyalkenes; poly(vinyl fluoride); PTFE; polyarylethyl ketone PAEK; polyphenylene and mixtures thereof.
[0114] If a ceramic is chosen as the material of construction for a component, then the ceramic is preferably selected from the group consisting of alumina, zirconia and mixtures thereof. It is preferred to select an alumina-zirconia ceramic, such as BIOLOX delta™, available from CeramTec of Plochingen, Germany.
[0115] In some embodiments, the cage member comprises PEEK. In others, it is a ceramic.
[0116] In some embodiments, the first component consists essentially of a metallic material, preferably a titanium alloy or a chrome-cobalt alloy.
[0117] In some embodiments, the components are made of a stainless steel alloy, preferably BioDur® CCM Plus® Alloy available from Carpenter Specialty Alloys, Carpenter Technology Corporation of Wyomissing, Pa. In some embodiments, the outer surfaces of the components are coated with a sintered beadcoating, preferably Porocoat™, available from DePuy Orthopaedics of Warsaw, Ind.
[0118] In some embodiments, the components are made from a composite comprising carbon fiber. Composites comprising carbon fiber are advantageous in that they typically have a strength and stiffness that is superior to neat polymer materials such as a polyarylethyl ketone PAEK. In some embodiments, each component is made from a polymer composite such as a PEKK-carbon fiber composite.
[0119] Preferably, the composite comprising carbon fiber further comprises a polymer. Preferably, the polymer is a polyarylethyl ketone (PAEK). More preferably, the PAEK is selected from the group consisting of polyetherether ketone (PEEK), polyether ketone ketone (PEKK) and polyether ketone (PEK). In preferred embodiments, the PAEK is PEEK.
[0120] In some embodiments, the carbon fiber comprises between 1 vol % and 60 vol % (more preferably, between 10 vol % and 50 vol %) of the composite. In some embodiments, the polymer and carbon fibers are homogeneously mixed. In others, the material is a laminate. In some embodiments, the carbon fiber is present in a chopped state. Preferably, the chopped carbon fibers have a median length of between 1 mm and 12 mm, more preferably between 4.5 mm and 7.5 mm. In some embodiments, the carbon fiber is present as continuous strands.
[0121] In especially preferred embodiments, the composite comprises: [0119] 40-99% (more preferably, 60-80 vol %) polyarylethyl ketone (PAEK), and [0120] 1-60% (more preferably, 20-40 vol %) carbon fiber, wherein the polyarylethyl ketone (PAEK) is selected from the group consisting of polyetherether ketone (PEEK), polyether ketone ketone (PEKK) and polyether ketone (PEK).
[0122] In some embodiments, the composite consists essentially of PAEK and carbon fiber. More preferably, the composite comprises 60-80 wt % PAEK and 20-40 wt % carbon fiber. Still more preferably the composite comprises 65-75 wt % PAEK and 25-35 wt % carbon fiber.
[0123] In some embodiments, the post and screw components of the present invention are made from a biocompatible metal, such as stainless steel, chromium cobalt, or titanium alloy.
[0124] In some embodiments, the plates of the present invention are made from a biocompatible metal, such as stainless steel, chromium cobalt, or titanium alloy.
[0125] Although the present invention has been described with reference to its preferred embodiments, those skillful in the art will recognize changes that may be made in form and structure which do not depart from the spirit of the invention.
[0126] In some embodiments, the central throughhole of the cage is filled with a fusion material. This fusion material promotes bony fusion of the adjacent vertebral bodies through the disc space. In some embodiments, the fusion material may be autograft bone marrow or allograft bone. In some embodiments, the fusion material may be synthetic, such as tricalcium phosphate or hydroxyapatite. In some embodiments, the fusion material may be a recombinant protein, such as a growth factor.
Implant Placement without a Plate Cage Connection
[0127] After successfully accessing, clearing and sizing the disc space, select the corresponding implant, fill the cage implant with autogenous bone graft material and attach to the inserter. Gently impact the cage implant into the disc space while monitoring placement under AP fluoroscopy. Ideal placement of the implant is to support the endplate medial/laterally to the contra-lateral rim and between the anterior third and middle third of the disc space from an anterior/posterior perspective.
[0128] Select the appropriate nubbed plate implant based on morphology and cage size, attach it to its respective inserter. Using the cage as a guide, insert the plate until the nubbed portion is within the disc space supporting the vertebral body rim and the plate portion abuts the ipsilateral walls of the superior and inferior vertebral bodies. The nubbed plate can be slightly repositioned from the cage location anteriorly or posteriorly in order to optimize the screw location or to account for anomalies such as osteophytes or a slightly compromised cage trajectory.
[0129] Attach the plate with the appropriate anchors.
Implant Placement with the Plate and Cage Connected
[0130] After successfully accessing, clearing and sizing the disc space, select the corresponding implant, fill the cage portion with autogenous bone graft material and attach the plate-cage combination to the inserter. Gently impact the implant into the disc space while monitoring placement under AP fluoroscopy. Ideal placement of the implant is for the cage portion to support the endplate medial/laterally to the contra-lateral rim and for the nubbed portion to support the ipsilateral rim while the plate portion is in contact with the walls of the superior and inferior vertebral bodies. The implant should be between the anterior third and middle third of the disc space from an anterior/posterior perspective.
[0131] The nubbed plate portion can only be slightly repositioned from the cage based on the extent of the polyaxial/sliding connection between the plate and nubbed portion. This allows for a diminished ability to accommodate morphological or surgical anomalies but increases the ergonomics of the surgery by reducing it to a single insertion technique.
[0132] Attach the plate with the appropriate anchors.
[0133] In some embodiments, the nub supports the ipsilateral rim of the vertebral body and the cage supports the contralateral rim of the vertebral body.