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, a transverse aperture through each lateral side, which extends the entire transverse length of the body and nearly the entire height of the implant body, a posterior portion, an anterior portion comprising a solid rear wall extending substantially the entire width and height of the body, 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 blunt and radiused portion along the top of the anterior portion, wherein the portion of the transverse rim that is not blunt and radiused has a roughened surface topography, wherein the blunt and radiused portion does not include any roughened surface topography, and wherein the body has a sharp edge for digging into vertebral end plate bone and resisting expulsion of the implant.
2. The interbody spinal implant of claim 1 , wherein the body comprises metal.
3. The interbody spinal implant of claim 1 , wherein the body comprises a non-metal polymer.
4. The interbody spinal implant of claim 3 , wherein the non-metal polymer is selected from the group consisting of polyetherether-ketone, and ultra-high molecular weight polyethylene.
5. The interbody spinal implant of claim 1 , wherein the body comprises a composite of metal and a non-metal polymer.
6. The interbody spinal implant of claim 1 , wherein the solid rear wall closes the anterior portion of the body.
7. The interbody spinal implant of claim 1 , wherein the spinal implant comprises a lordotic angle adapted to facilitate alignment of the spine.
8. The interbody spinal implant of claim 1 , further comprising bone graft material disposed in the substantially hollow center.
9. The interbody 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 a combination thereof.
10. The interbody spinal implant of claim 1 , wherein the posterior portion comprises an opening for engaging a surgical tool.
11. An interbody spinal implant, comprising a body that is generally box-shaped in transverse cross section, and comprises: a top surface, a bottom surface, opposing lateral sides, a transverse aperture through each lateral side, which extends the entire transverse length of the body and nearly the entire height of the implant body, a posterior portion, an anterior portion comprising a solid rear wall extending substantially the entire width and height of the body, 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 blunt and radiused portion along the top of the anterior portion, wherein the portion of the transverse rim that is not blunt and radiused has a roughened surface topography, wherein the blunt and radiused portion does not include any roughened surface topography, and wherein the body has a sharp edge for digging into vertebral end plate bone and resisting expulsion of the implant.
12. The interbody spinal implant of claim 11 , wherein the body comprises metal.
13. The interbody spinal implant of claim 11 , wherein the body comprises a non-metal polymer.
14. The interbody spinal implant of claim 13 , wherein the non-metal polymer is selected from the group consisting of polyetherether-ketone, and ultra-high molecular weight polyethylene.
15. The interbody spinal implant of claim 11 , wherein the body comprises a composite of metal and a non-metal polymer.
16. The interbody spinal implant of claim 11 , wherein the solid rear wall closes the anterior portion of the body.
17. The interbody spinal implant of claim 11 , wherein the spinal implant comprises a lordotic angle adapted to facilitate alignment of the spine.
18. The interbody spinal implant of claim 11 , further comprising bone graft material disposed in the substantially hollow center.
19. The interbody spinal implant of claim 18 , 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 a combination thereof.
20. The interbody spinal implant of claim 11 , wherein the posterior portion comprises an opening for engaging a surgical tool.
21. The interbody spinal implant of claim 11 , wherein the body comprises a D-shaped box in transverse cross-section, wherein the transverse rim comprises a curved anterior portion and a substantially flat posterior portion, thereby forming the D-shaped box.