A61F2002/30973

Spinal implant system and method
10413427 · 2019-09-17 · ·

A spinal implant system includes at least one interbody implant having a first member including a tissue engaging surface and at least one mating element. A second member includes a tissue engaging surface and at least one mating element. An intermediate member includes at least one mating element. An intra-operative surgical tool is connectable with at least one of the members to engage adjacent mating elements and fix the intermediate member with at least one of the first member and the second member. Implants, surgical instruments and methods are disclosed.

Coated hemi-prosthesis implant
10350071 · 2019-07-16 · ·

A hemi-prosthesis implant comprises a replacement-joint part with an articulation surface for tribological pairing with a joint surface of a natural joint counterpart. The articulation surface is embodied with a coating applied on a substrate. The substrate provides a relief for the adhesion of the coating. The relief may comprise one or more of a plurality of grooves, a plurality of teeth, a ribbing, and a roughened surface. The relief may be embodied entirely or partially outside the articulation surface. The replacement joint part may optionally comprise a ventilation feature, and the articulation surface may be formed by injection molding on the substrate. The hemi-prosthesis implant may be part of an implant set that includes both a hemi-prosthesis implant and a total prosthesis implant, either of which can be chosen intraoperatively.

THREADED COMPOSITE INTERBODY DEVICE AND ASSOCIATED MANUFACTURING METHOD
20190159900 · 2019-05-30 ·

A composite threaded interbody device includes (a) an outer surface that is cylindrical or conical, (b) a plastic core having two outer sections, each of the outer sections forming a respective portion of the outer surface and spanning a respective azimuthal range in an azimuthal dimension relative to a longitudinal axis of the outer surface, the outer sections being separated from each other in the azimuthal dimension by two recessed sections that are recessed from the outer surface, and (c) two threaded endplates coupled to the two recessed sections and spanning gaps between the outer sections, to complete the outer surface.

Implantable medical devices

Implantable medical devices are provided. In one embodiment, a device includes a body having an external surface defining an outer profile of the device. The body includes a porous matrix including a series of interconnected macropores defined by a plurality of interconnected struts each including a hollow interior. A filler material substantially fills at least a portion of the series of interconnected macropores. The external surface of the body includes a plurality of openings communicating with the hollow interior of at least a portion of the plurality of interconnected struts. In a further aspect of this embodiment, the external surface includes exposed areas of the filler material and porous matrix in addition to the exposed openings. In another aspect, the porous matrix is formed from a bioresorbable ceramic and the filler material is a biologically stable polymeric material. Still, other aspects related to this and other embodiments are also disclosed.

CAGE FOR VERTEBRAL ARTHRODESIS OPERATIONS
20240180713 · 2024-06-06 ·

A cage for vertebral arthrodesis operations has a body with a first surface for contact with an endplate and a second surface for contact with a second endplate, the surfaces arranged opposite each other in a coronal heightwise direction of the cage, an entry side for entry into the intervertebral disc space and a pushing side opposite the entry side in a direction of insertion into the intervertebral disc space.

The cage has a continuous directional guide relief on one of two opposite surfaces for contact with a vertebral endplate; during insertion of the cage between the vertebral endplates from the entry side by means of action on the pushing side, the directional guide relief guides the cage along a predefined movement trajectory for insertion of the cage between the first vertebral endplate and the second vertebral endplate, from an entry point to a predefined and correct end position.

Methods and devices for intracorporeal bonding of implants with thermal energy

The present invention provides a method for stabilizing a fractured bone. The method includes positioning an elongate rod in the medullary canal of the fractured bone and forming a passageway through the cortex of the bone. The passageway extends from the exterior surface of the bone to the medullary canal of the bone. The method also includes creating a bonding region on the elongate rod. The bonding region is generally aligned with the passageway of the cortex. Furthermore, the method includes positioning a fastener in the passageway of the cortex and on the bonding region of the elongate rod and thermally bonding the fastener to the bonding region of the elongate rod while the fastener is positioned in the passageway of the cortex.

COATED HEMI-PROSTHESIS IMPLANT
20190151097 · 2019-05-23 · ·

A hemi-prosthesis implant comprises a replacement-joint part with an articulation surface for tribological pairing with a joint surface of a natural joint counterpart. The articulation surface is embodied with a coating applied on a substrate. The substrate provides a relief for the adhesion of the coating. The relief may comprise one or more of a plurality of grooves, a plurality of teeth, a ribbing, and a roughened surface. The relief may be embodied entirely or partially outside the articulation surface. The replacement joint part may optionally comprise a ventilation feature, and the articulation surface may be formed by injection molding on the substrate. The hemi-prosthesis implant may be part of an implant set that includes both a hemi-prosthesis implant and a total prosthesis implant, either of which can be chosen intraoperatively.

Intervertebral devices

An intervertebral fusion device is disclosed. The intervertebral fusion device comprises a superior component (40), an inferior component (60) and a core component (10). The superior component (40) has a superior component top side and a superior component bottom side and is configured to be received in an intervertebral space between first and second vertebrae whereby the superior component top side abuts against the first vertebra. The inferior component (60) has an inferior component top side and an inferior component bottom side and is configured to be received in the intervertebral space whereby the inferior component bottom side abuts against the second vertebra. The superior component bottom side and the inferior component top side oppose each other when the superior and inferior components (40, 60) are received in the intervertebral space. The core component (10) is configured for insertion between the superior and inferior components (40, 60) whereby a separation between the superior and inferior components is determined. The core component (10) comprises a retention mechanism which moves between a contracted condition and an expanded condition. The core component (10) is insertable between the superior and inferior components (40, 60) when the retention mechanism is in the contracted condition. The retention mechanism inter-engages with the superior component (40) and the inferior component (60) when in the expanded condition and when the core component (10) is received between the superior and inferior components to thereby present resistance to movement of the core component from between the superior and inferior components.

MODULAR FEMORAL NAIL AND METHOD OF USE THEREOF

An intramedullary nail for implantation within a fractured bone. The intramedullary nail includes two or more nail modules. Each nail module has an elongated body with a first end and a second end. For each nail module, at least one of the first end or the second end is a connecting end configured to connect to a second connecting end on a second nail module.

Composite porous interbodies and methods of manufacture

A method of forming a composite titanium body for use in forming spinal implant interbodies includes selecting a metal alloy body, carving out a top portion and a bottom portion from the metal alloy body, and bonding a porous material to the carved-out top and bottom portions. Multiple pieces may be cut from the composite titanium body, each having a front face formed of the metal alloy, top and bottom portions formed of the porous material, and with a medial portion of the metal alloy extending from the front face to the back. Methods and devices for spinal interbodies having locking mechanisms to prevent bone screw back-out are also described.