Spinal implant having variable ratios of the integration surface area to the axial passage area
View Patent ↗An interbody spinal implant including a body having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, and a substantially hollow center in communication with a vertical aperture. The body, vertical aperture, and bone contact surfaces of the implant each have a surface area that may be independently varied to enhance load support and facilitate implant integration with vertebral bone.
1. An interbody spinal implant, comprising:
a body having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, a single vertical aperture extending from the top surface to the bottom surface, defining a perimeter, and having a shape, dimensions, and position on the top surface and the bottom surface that define a transverse rim with a varying thickness on the top surface and on the bottom surface of the body, having a maximum width at its center, between the opposing lateral sides, and tapering inwardly from the center to each of its ends, one end proximate the anterior portion and the other end proximate the posterior portion, and a surface area of about 120 mm 2 to about 1200 mm 2 ,
wherein at least a portion of the transverse rim comprises a vertebral endplate bone contact surface comprising a roughened surface topography, without teeth, surrounding the entire perimeter of the vertical aperture, and having a surface area of about 60 mm 2 to about 600 mm 2 ,
the body having generally rounded and blunt intersections defined along the entire lengths between the top surface and the lateral sides and the bottom surface and the lateral sides; and
the body having at least one sharp edge between the top and bottom surfaces and the anterior portion or the posterior portion.
2. The interbody spinal implant of claim 1 , wherein the vertebral endplate bone contact surface comprises a surface area of about 60 mm 2 to about 140 mm 2 .
3. The interbody spinal implant of claim 1 , wherein the vertebral endplate bone contact surface comprises a surface area of about 90 mm 2 to about 135 mm 2 .
4. The interbody spinal implant of claim 1 , wherein the vertebral endplate bone contact surface comprises a surface area of about 240 mm 2 to about 350 mm 2 .
5. The interbody spinal implant of claim 1 , wherein the vertebral endplate bone contact surface comprises a surface area of about 290 mm 2 to about 550 mm 2 .
6. The interbody spinal implant of claim 1 , wherein the implant comprises a ratio of the surface area of the single vertical aperture to the surface area of the body of about 5% to about 30%.
7. The interbody spinal implant of claim 1 , wherein the implant comprises a ratio of the surface area of the single vertical aperture to the surface area of the body of about 10% to about 35%.
8. The interbody spinal implant of claim 1 , wherein the implant comprises a ratio of the surface area of the single vertical aperture to the surface area of the body of about 20% to about 60%.
9. The interbody spinal implant of claim 1 , wherein the implant comprises a ratio of the surface area of the single vertical aperture to the surface area of the body of about 30% to about 65%.
10. The interbody spinal implant of claim 1 , wherein the implant comprises a ratio of the surface area of the single vertical aperture to the surface area of the body of about 40% to about 55%.
11. The interbody spinal implant of claim 1 further comprising bone growth material disposed in the single vertical aperture.
12. The interbody spinal implant of claim 1 , wherein the transverse rim comprises an anterior portion width, a posterior portion width, a first lateral side width, and a second lateral side width, and wherein the anterior portion width is different from the posterior portion width or the first lateral side width is different from the second lateral side width.
13. An interbody spinal implant, comprising:
a body having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, a substantially hollow center, a single vertical aperture extending from the top surface to the bottom surface, defining a perimeter, and having a surface area of about 120 mm 2 to about 1200 mm 2 ;
a first integration plate having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, and a single vertical aperture extending from the top surface to the bottom surface of the first integration plate and aligning with the single vertical aperture of the body,
optionally, a second integration plate having a top surface, a bottom surface, opposing lateral sides, opposing anterior and posterior portions, and a single vertical aperture extending from the top surface to the bottom surface of the second integration plate and aligning with the single vertical aperture of the body,
wherein the single vertical aperture of the first integration plate has a shape, dimensions, and position that define a first transverse rim with a varying thickness on the top surface of the first integration plate, having a maximum width at its center, between the opposing lateral sides, and tapering inwardly from the center to each of its ends, one end proximate the anterior portion and the other end proximate the posterior portion, and wherein at least a portion of the first transverse rim comprises a vertebral endplate bone contact surface comprising a roughened surface topography, without teeth, surrounding the entire perimeter of the vertical aperture, and having a surface area of about 60 mm 2 to about 600 mm 2 ,
and optionally wherein the single vertical aperture of the second integration plate has a shape, dimensions, and position that define a second transverse rim with a varying thickness on the top surface of the second integration plate, having a maximum width at its center, between the opposing lateral sides, and tapering inwardly from the center to each of its ends, one end proximate the anterior portion and the other end proximate the posterior portion, and wherein at least a portion of the second transverse rim comprises a vertebral endplate bone contact surface comprising a roughened surface topography, without teeth, surrounding the entire perimeter of the vertical aperture, and having a surface area of about 60 mm 2 to about 600 mm 2 ,
the body having generally rounded and blunt intersections defined along the entire lengths between the top surface and the lateral sides and the bottom surface and the lateral sides; and
the first integration plate and optionally the second integration plate having at least one sharp edge between the top surface and the anterior portion or the posterior portion.
14. The interbody spinal implant of claim 13 , wherein the vertebral endplate bone contact surface of the first transverse rim, and optionally of the second transverse rim, comprises a surface area of about 60 mm 2 to about 140 mm 2 .
15. The interbody spinal implant of claim 13 , wherein the vertebral endplate bone contact surface of the first transverse rim, and optionally of the second transverse rim, comprises a surface area of about 90 mm 2 to about 135 mm 2 .
16. The interbody spinal implant of claim 13 , wherein the vertebral endplate bone contact surface of the first transverse rim, and optionally of the second transverse rim, comprises a surface area of about 240 mm 2 to about 350 mm 2 .
17. The interbody spinal implant of claim 13 , wherein the vertebral endplate bone contact surface of the first transverse rim, and optionally of the second transverse rim, comprises a surface area of about 290 mm 2 to about 550 mm 2 .
18. The interbody spinal implant of claim 13 , wherein the implant comprises a ratio of the surface area of the single vertical aperture of the first integration plate, and optionally of the single vertical aperture of the second integration plate, to the surface area of the body of about 5% to about 30%.
19. The interbody spinal implant of claim 13 , wherein the implant comprises a ratio of the surface area of the single vertical aperture of the first integration plate, and optionally of the single vertical aperture of the second integration plate, to the surface area of the body of about 10% to about 35%.
20. The interbody spinal implant of claim 13 , wherein the implant comprises a ratio of the surface area of the single vertical aperture of the first integration plate, and optionally of the single vertical aperture of the second integration plate, to the surface area of the body of about 20% to about 60%.
21. The interbody spinal implant of claim 13 , wherein the implant comprises a ratio of the surface area of the single vertical aperture of the first integration plate, and optionally of the single vertical aperture of the second integration plate, to the surface area of the body of about 30% to about 65%.
22. The interbody spinal implant of claim 13 , wherein the implant comprises a ratio of the surface area of the single vertical aperture of the first integration plate, and optionally of the single vertical aperture of the second integration plate, to the surface area of the body of about 40% to about 55%.
23. The interbody spinal implant of claim 13 further comprising bone growth material disposed in the single vertical aperture of the body, the single vertical aperture of the first integration plate, the single vertical aperture of the second integration plate, or all three single vertical apertures.
24. The interbody spinal implant of claim 13 , wherein the first transverse rim, the second transverse rim, or both transverse rims comprise an anterior portion width, a posterior portion width, a first lateral side width, and a second lateral side width, and wherein the anterior portion width is different from the posterior portion width or the first lateral side width is different from the second lateral side width.