Asymmetrically expandable cage
The present disclosure describes an intervertebral implant having a laterovertically-expanding shell operable for a reversible expansion from a collapsed state into an expanded state, the laterovertically-expanding shell having one or more connectors, and a pair of lateral extension elements that function to laterally expand the footprint of the implant within an intervertebal disc space.
1. A surgical implant configured for placement within an intervertebral space, comprising:
a laterovertically-expanding shell having a longitudinal axis and configured to create an intervertebral scaffolding system in vivo, the shell having a first body portion configured to engage a first vertebral endplate and a second body portion configured to engage a second vertebral endplate, the shell further including a collapsed state and an expanded state;
wherein the shell is configured to extend asymmetrically from the longitudinal axis, extending further in a first lateral direction than in a second lateral direction to bias a profile of the implant in the first lateral direction when the shell is in the expanded state; and
wherein the first body portion includes a first elongated support beam extending parallel to the longitudinal axis, a second elongated support beam laterally displaced from the first elongated support beam and extending parallel to the longitudinal axis, and a plurality of connectors extending between the first and second elongated support beams.
2. The surgical implant of claim 1 , wherein the second body portion includes a third elongated support beam extending parallel to the longitudinal axis, a fourth elongated support beam laterally displaced from the third elongated support beam and extending parallel to the longitudinal axis, and a plurality of connectors extending between the third and fourth elongated support beams.
3. The surgical implant of claim 2 , wherein each of the first and second support beams has a length and an edge, and one of the first and second support beams includes a first lateral extension element extending in a direction away from the other of the first and second support beams, the first lateral extension element having a length dimension extending at least substantially the length of the respective support beam and a width dimension extending laterally away from the edge of the respective support beam.
4. The surgical implant of claim 3 , wherein each of the third and fourth support beams has a length and an edge, and one of the third and fourth support beams includes a second lateral extension element extending in a direction away from the other of the third and fourth support beams, the second lateral extension element having a length dimension extending at least substantially the length of the respective support beam and a width dimension extending laterally away from the edge of the respective support beam.
5. The surgical implant of claim 4 , wherein the first and second lateral extension elements extend in the same direction.
6. The surgical implant of claim 4 , wherein the respective support beams having the first and second lateral extension elements each have a width dimension that is between 1.2 and 10 times greater than the width dimensions of the other respective support beams.
7. The surgical implant of claim 1 , wherein the shell is made from at least one of a polymer, metal alloy, and titanium alloy.
8. The surgical implant of claim 1 , wherein the connectors are bowed in a proximal direction.
9. The surgical implant of claim 8 , wherein the bowed connectors maintain a curved orientation at the apex of the bowed shape to prevent stress cracking.
10. A surgical implant configured for placement within an intervertebral space, comprising:
a laterovertically-expanding shell, the shell having a longitudinal axis and configured to create an intervertebral scaffolding system in vivo, the shell having a first body portion configured to engage a first vertebral endplate and a second body portion configured to engage a second vertebral endplate, the shell further including a collapsed state and an expanded state;
wherein the shell is configured to extend asymmetrically from the longitudinal axis, extending further in a first lateral direction than in a second lateral direction to bias a profile of the implant in the first lateral direction when the shell is in the expanded state; and
wherein the shell includes a central layer and a plurality of surface layers, the central layer and surface layers comprising different materials.
11. The surgical implant of claim 10 , wherein the central layer is made from a medical grade polymer.
12. The surgical implant of claim 11 , wherein the medical grade polymer is one of PEEK, polyetherimide, polyimide, and polyamide.
13. The surgical implant of claim 10 , wherein the surface layers are made from at least one of titanium alloy, cobalt chromium, stainless steel, ceramic, silicon nitride, and hydroxyapatite.
14. A surgical implant having a combination of materials combined in layers, comprising:
a laterovertically-expanding shell having a distal region and configured to create an intervertebral scaffolding system in vivo, the shell having a layered assembly that includes a central layer and a plurality of surface layers; wherein
the central layer has a top face and a bottom face, and is configured to associate with the plurality of surface layers;
the plurality of surface layers has a top surface layer and a bottom surface layer, the top surface layer configured to associate with the top face of the central layer and form a first body portion configured to engage a first vertebral endplate; and the bottom surface layer configured to associate with the bottom face of the central layer and form a second body portion configured to engage a second vertebral endplate; and
the shell has a collapsed state and an expanded state;
wherein the central layer and the plurality of surface layers comprise different materials.
15. The surgical implant of claim 14 , wherein the central layer is made from a medical grade polymer.
16. The surgical implant of claim 15 , wherein the medical grade polymer is one of PEEK, polyetherimide, polyimide, and polyamide.
17. The surgical implant of claim 14 , wherein the surface layers are made from at least one of titanium alloy, cobalt chromium, stainless steel, ceramic, silicon nitride, and hydroxyapatite.
18. The surgical implant of claim 14 , wherein the surface layers have at least one of a roughened and porous texture.
19. The surgical implant of claim 14 , wherein the surface layers are associated with the central layer using at least one of pressure, heat melting, snap fit engagement, and adhesive.