Abstract: A non-suture soft tissue anchor device is disclosed, which is used in orthopedic surgical cases for attaching tendons and ligaments (i.e., soft tissue) to bone. The non-suture soft tissue anchor device comprises a body component configured in an oval shape. Further, the body component comprises at least two through-holes, with one through-hole positioned on each opposing narrow end of the body component. The through-holes are sized and shaped to accept a bone screw to secure the device to the bone. Further, the body component comprises two or more slots to accept the soft tissue. Specifically, the soft tissue is weaved through the slots like a belt buckle to lock the soft tissue in place. The soft tissue is locked in place at a set tension. The slots define a moveable lock bar, which further locks the soft tissue between the bone and the device.

Abstract: A subchondral implant and subchondral implant system are disclosed, and are designed as a bone void filler for damaged bone tissue. The subchondral implant comprises a body component configured in a cylindrical shape with a hollow interior cavity and an exterior curved sidewall. The curved sidewall includes a plurality of helical ribs in a spaced apart manner for optimal fixation. The top surface comprises a plurality of through-holes for sutures, when securing tissue graft. An adjacent subchondral implant can be utilized with the subchondral implant and is nested against it for use. The nested implants allow users to repair large, elongated areas that may not be repaired by a single subchondral implant.

Abstract: A subchondral implant is disclosed, which is designed as a bone void filler for damaged bone tissue. The subchondral implant comprises a body component configured in a cylindrical shape with a hollow interior cavity and an exterior curved sidewall. The curved sidewall includes a plurality of helical ribs in a spaced apart manner for optimal fixation. The top surface comprises a plurality of through-holes for sutures, when securing tissue graft. An adjacent subchondral implant can be utilized with the subchondral implant and is nested against it for use. The nested implants allow users to repair large, elongated areas that may not be repaired by a single subchondral implant.

Abstract: A subchondral implant is disclosed, which is designed as a bone void filler for damaged bone tissue. The subchondral implant comprises a body component configured in a cylindrical shape with a hollow interior cavity and an exterior curved sidewall. The curved sidewall includes a plurality of helical ribs in a spaced apart manner for optimal fixation. The top surface comprises a plurality of through-holes for sutures, when securing tissue graft. An adjacent subchondral implant can be utilized with the subchondral implant and is nested against it for use. The nested implants allow users to repair large, elongated areas that may not be repaired by a single subchondral implant.

Abstract: The present invention relates to a patient specific instrumentation for a total ankle replacement. The system is comprised of a device primarily comprised of a device front face; a device rear face opposite the front face that may be configured to face a human tibia; a device thickness extending from the device front face to the device rear face; a device top; a device bottom that may configured to be positioned over a user's foot; a device height extending from the device top to the device bottom and perpendicular to device thickness; a device left side; a device right side; a device width extending from the device left side to the device right side and perpendicular to the device height and device thickness; and a lower portion that may include a device body.

Abstract: The present invention relates to a patient specific instrumentation for a total ankle replacement. The system is comprised of a device primarily comprised of a device front face; a device rear face opposite the front face that may be configured to face a human tibia; a device thickness extending from the device front face to the device rear face; a device top; a device bottom that may configured to be positioned over a user's foot; a device height extending from the device top to the device bottom and perpendicular to device thickness; a device left side; a device right side; a device width extending from the device left side to the device right side and perpendicular to the device height and device thickness; and a lower portion that may include a device body.