Interbody spinal implant having a roughened surface topography
View Patent ↗An interbody spinal implant including a body having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, and a single vertical aperture. The single vertical aperture extends from the top surface to the bottom surface, has a size and shape predetermined to maximize the surface area of the top surface and the bottom surface available proximate the anterior and posterior portions while maximizing both radiographic visualization and access to the substantially hollow center, and defines a transverse rim. The body may be non-metallic and may form one component of a composite implant; the other component is a metal plate disposed on at least one of the top and bottom surfaces of the body.
1. An interbody spinal implant, comprising:
a body that is generally oval-shaped in transverse cross section, and comprises: a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, and a single vertical aperture, extending from the top surface to the bottom surface, having maximum width at its center, and defining a transverse rim on the top surface and on the bottom surface, said transverse rim having a posterior thickness greater than an anterior thickness, and having a blunt and radiused portion along the top of each lateral side and the top of the posterior portion, wherein the portion of the transverse rim that is not blunt and radiused has a roughened surface topography adapted to grip bone and inhibit migration of the implant, wherein the blunt and radiused portion does not include any roughened surface topography, and wherein the body has a sharp edge at the junction of the anterior portion and the top surface and at the junction of the anterior portion and the bottom surface to resist pullout of the implant once inserted in the intervertebral space.
2. The spinal implant of claim 1 wherein the body is metal.
3. The spinal implant of claim 1 , wherein the body is a non-metal selected from polyetherether-ketone, hedrocel, and ultra-high molecular weight polyethylene.
4. The spinal implant of claim 1 , wherein the body is a composite formed, in part, of metal and, in part, of a non-metal selected from polyetherether-ketone, hedrocel, and ultra-high molecular weight polyethylene.
5. The spinal implant of claim 1 , wherein the body has at least one transverse aperture extending at least partially along the transverse length of the body.
6. The spinal implant of claim 1 , wherein the posterior portion has a generally tapered nose.
7. The spinal implant of claim 1 , wherein the spinal implant comprises a lordotic angle adapted to facilitate alignment of the spine.
8. The spinal implant of claim 1 , further comprising bone graft material disposed in the substantially hollow center and adapted to facilitate the formation of a solid fusion column within the spine.
9. The spinal implant of claim 8 , wherein the bone graft material is cancellous autograft bone, allograft bone, demineralized bone matrix (DBM), porous synthetic bone graft substitute, bone morphogenic protein (BMP), or combinations thereof.
10. The spinal implant of claim 8 , further comprising a wall closing at least one of the opposing anterior and posterior portions to contain the bone graft material.
11. The spinal implant of claim 8 , wherein the anterior portion has an opening achieving one or more of the following functions: being adapted to engage a delivery device, facilitating delivery of bone graft material to the substantially hollow center, enhancing visibility of the implant, and providing access to the bone graft material.
12. An interbody spinal implant, comprising:
a body that is generally rectangular-shaped in transverse cross section, and comprises a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, and a single vertical aperture, extending from the top surface to the bottom surface, having maximum width at its center, and defining a transverse rim on the top surface and on the bottom surface, said transverse rim having an anterior thickness greater than a posterior thickness, and having a blunt and radiused portion along the top of each lateral side and the top of the anterior portion, wherein the portion of the transverse rim that is not blunt and radiused has a roughened surface topography adapted to grip bone and inhibit migration of the implant, wherein the blunt and radiused portion does not include any roughened surface topography, wherein the body has a sharp edge at the junction of the posterior portion and the to surface and at the junction of the posterior portion and the bottom surface to resist pullout of the implant once inserted in the intervertebral space.
13. The interbody spinal implant of claim 12 , wherein the body is metal.
14. The interbody spinal implant of claim 12 , wherein the body is a non-metal selected from polyetherether-ketone, hedrocel, and ultra-high molecular weight polyethylene.
15. The spinal implant of claim 12 , wherein the spinal implant comprises a lordotic angle adapted to facilitate alignment of the spine.
16. The spinal implant of claim 12 , further comprising bone graft material disposed in the substantially hollow center and adapted to facilitate the formation of a solid fusion column within the spine.
17. The spinal implant of claim 16 , wherein the bone graft material is cancellous autograft bone, allograft bone, demineralized bone matrix (DBM), porous synthetic bone graft substitute, bone morphogenic protein (BMP), or combinations thereof.
18. An interbody spinal implant, comprising:
a body that is generally curved-shaped in transverse cross section, and comprises a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, and a single vertical aperture extending from the top surface to the bottom surface, having maximum width at its center, and defining a transverse rim on the top surface and on the bottom surface, said transverse rim having a posterior thickness greater than an anterior thickness, and having a blunt and radiused portion along the top of each lateral side and the top of the posterior portion, wherein the portion of the transverse rim that is not blunt and radiused has a roughened surface topography adapted to grip bone and inhibit migration of the implant, wherein the blunt and radiused portion does not include any roughened surface topography, and wherein the body has a sharp edge at the junction of the anterior portion and the to surface and at the junction of the anterior portion and the bottom surface to resist pullout of the implant once inserted in the intervertebral space.
19. The interbody spinal implant of claim 18 , wherein the body is metal.
20. The interbody spinal implant of claim 18 , wherein the body is a non-metal selected from polyetherether-ketone, hedrocel, and ultra-high molecular weight polyethylene.
21. The spinal implant of claim 18 , wherein the spinal implant comprises a lordotic angle adapted to facilitate alignment of the spine.
22. The spinal implant of claim 18 , further comprising bone graft material disposed in the substantially hollow center and adapted to facilitate the formation of a solid fusion column within the spine.
23. The spinal implant of claim 22 , wherein the bone graft material is cancellous autograft bone, allograft bone, demineralized bone matrix (DBM), porous synthetic bone graft substitute, bone morphogenic protein (BMP), or combinations thereof.