Stenotic device
View Patent ↗A spinal implant is configured to be received between bony spinal protrusions of adjacent vertebrae particularly, but not necessarily, in the lumbar region of the spine and hold them apart. The spinal implant may be used interlaminar, interbody or interbony protrusion. The present bony spinal protrusion spacer is not fixed to any bony structures of the vertebrae and, as such, use of the present bony spinal protrusion spacer does not result in fusion. It may therefore be removed if necessary. Attachment structures formed as part of the bony spinal protrusion spacer receive and engage portions of adjacent bony protrusions. The attachment structures provide one or more ridges, bumps, protrusions, projections, lips, flanges, overhangs, overhangs that are threadably engaged, extensions and/or the like that form one or more pockets or cavities into which portions of adjacent bony spinal protrusions are separately lodged and held. In this manner (via retention of the bony spinal protrusions), appropriate and/or desired spacing between adjacent vertebrae is maintained. As such, the present bony spinal protrusion spacer is designed to remain safely and permanently in place without attaching to the bone or ligaments of the back.
1. A spinal implant comprising:
a body having a first D-shaped portion, a second D-shaped portion spaced apart from the first D-shaped portion, a side portion, and a protuberance, wherein the side portion and the protuberance extend between the first D-shaped portion and the second D-shaped portion, wherein the protuberance includes a first bump and a second bump extending in different directions and disposed apart from the side portion;
an upper opening in the body to provide access to a first substantially enclosed cavity defined by the first D-shaped portion, the second D-shaped portion, the protuberance, the side portion, and the first bump;
a lower opening in the body to provide access to a second substantially enclosed cavity defined by the first D-shaped portion, the second D-shaped portion, the protuberance, the side portion, and the second bump;
wherein the first substantially enclosed cavity is configured to receive a portion of a first bony spinal protrusion of a first vertebra; and
wherein the second substantially enclosed cavity is configured to receive a portion of a second bony spinal protrusion of a second vertebra that is adjacent to the first vertebra.
2. The spinal implant of claim 1 , wherein the first bump is configured to prevent the body from moving relative to the first bony spinal protrusion, and the second bump is configured to prevent the body from moving relative to the second bony spinal protrusion.
3. The spinal implant of claim 1 , wherein the body is formed of a biocompatible material.
4. The spinal implant of claim 1 , wherein the upper opening faces the same direction as the first bump, and wherein the lower opening faces the same direction as the second bump.
5. A spinal implant comprising:
a body formed of a biocompatible material the body having:
a first side wall,
a second side wall spaced apart from the first side wall,
an end wall extending between the first side wall and the second side wall;
a protuberance extending between the first side wall and the side wall,
an attachment structure disposed in the opening and extending from the protuberance, the attachment structure having:
a first projection extending from the protuberance in a first direction and disposed apart from the end wall, and
a second projection extending from the protuberance in a second direction different than the first direction and disposed apart from the end wall,
a first opening in the body to provide access to a first substantially enclosed cavity defined by the first side wall, the second side wall, the protuberance, the end wall, and the first projection;
a second opening in the body to provide access to a second substantially enclosed cavity defined by the first side wall, the second side wall, the protuberance, the end wall, and the second projection;
wherein the first side wall, the second side wall, the protuberance, and the attachment structure define a cavity configured to receive and retain a first bony spinal protrusion of a first vertebra and a second bony spinal protrusion of a second vertebra that is adjacent the first vertebra.
6. The spinal implant of claim 5 , the first opening facing generally the same direction as the first projection, and wherein the second opening facing generally the same direction as the second projection.
7. The spinal implant of claim 5 , wherein at least one of the first side wall and the second side wall is D-shaped.
8. A spinal implant comprising:
a first portion having D-shaped surface;
a second portion having D-shaped surface generally parallel and spaced from the first portion so as to define an interior therebetween;
a side portion extending between the first portion and the second portion; and
a central structure formed in the interior and configured to receive and hold a first bony spinal protrusion of a first vertebra and a second bony spinal protrusion of a second vertebra that is adjacent the first vertebra, wherein the central structure comprises a protuberance with first and second projections extending in different directions to form a first cavity to receive the first vertebra and a second cavity to receive the second vertebra;
a first opening to provide access to a first substantially enclosed cavity defined by the first portion, the second portion, the protuberance, the side portion, and the first projection;
a second opening in the body to provide access to a second substantially enclosed cavity defined by the first side wall, the second side wall, the protuberance, the end wall, and the second ridge.
9. The spinal implant of claim 8 , wherein the central structure includes a bore configured to receive an insertion tool.
10. The spinal implant of claim 9 , wherein the central structure includes a pair of side bores adjacent to the bore.
11. A method for treating spinal stenosis comprising the steps of:
creating an opening proximate first and second stenotic vertebrae;
spreading the first and second stenotic vertebrae; and
inserting an implant between the first and second stenotic vertebrae, the implant configured to maintain a spacing between the first and second stenotic vertebrae and be held thereby, the implant comprising:
a body having a first D-shaped portion, a second D-shaped portion spaced apart from the first D-shaped portion, a side portion, and a protuberance, wherein the side portion and the protuberance extend between the first D-shaped portion and the second D-shaped portion, wherein the protuberance includes a first bump and a second bump extending in different directions and disposed apart from the side portion;
an upper opening in the body to provide access to a first substantially enclosed cavity defined by the first D-shaped portion, the second D-shaped portion, the protuberance, the side portion, and the first bump;
a lower opening in the body to provide access to a second substantially enclosed cavity defined by the first D-shaped portion, the second D-shaped portion, the protuberance, the side portion, and the second bump;
wherein the first substantially enclosed cavity is configured to receive a portion of a first bony spinal protrusion of a first vertebra; and
wherein the second substantially enclosed cavity is configured to receive a portion of a second bony spinal protrusion of a second vertebra that is adjacent to the first vertebra.