A61F2002/30004

Intervertebral fusion implant

The present invention provides an intervertebral implant for implantation in a treated area of an intervertebral space between vertebral bodies of a spine. The implant includes a spacer portion having an inferior and superior surface, wherein the inferior and superior surfaces each have a contact area capable of engaging with anatomy in the treated area, and the inferior and superior surfaces define a through-hole extending through the spacer body. The present invention further provides screw holes extending from a side portion to the inferior and superior surfaces of the spacer portion and a plate portion rigidly coupled to the spacer portion through a coupling means, wherein the plate portion contains screws holes for receiving screws. A screw back out prevention mechanism adapted on the plate portion and prevents the back out of screws from the screw holes.

GLENOSPHERE ASSEMBLY

Provided herein are various embodiments of an improved glenoid implant assembly that includes a baseplate, a polymer glenosphere, and an interfacing component. The interfacing component can be made of a material that is more rigid than the polymer glenosphere, has a bowl-shaped configuration with a convex side and a recessed side, where the convex side is configured to be secured to the circular recessed portion of the polymer glenosphere and the recessed side is configured to securely receive the baseplate. The interfacing component is interposed between the polymer glenosphere and the baseplate and provide a secure attachment between the polymer glenosphere and the baseplate.

Intervertebral Implant
20170143509 · 2017-05-25 ·

The intervertebral implant is in the form of a three-dimensional structure (10) comprising (a) a top side (1) and an underside (2) which are designed to rest against the end plates of two adjacent vertebras, (b) a left side face (3) and a right side face (4), (c) a front face (5) and a rear face (6), (d) a horizontal center plane situated between the top side (1) and the underside (2), (e) a vertical center plane (8) situated between the left side face (3) and the right side face (8) and (f) a plurality of boreholes (9) passing through the implant structure (10) that are designed to receive longitudinal affixation elements (20), the axes (19) of said elements intersecting the horizontal center plane (7). At least one of the boreholes (9) is designed in a manner that the affixation element (10) received in it can be rigidly connected to the intervertebral implant. Said connection is implemented using a thread or by matching conical surfaces.

Hybrid intervertebral disc spacer device and method of manufacturing the same

A hybrid spinal implant device, and method of making the same are disclosed. The spinal implant device comprises two facing endplates, each having at least one anchoring wall or pin element, and a plastic spacer anchored to and located between the two endplates. The endplates may be manufactured from titanium. The plastic spacer may be manufactured from a radiolucent, and bio-compatible polymer-based material including polyetheretherketone (PEEK), polyetherketone, polyetherketoneketone, and/or fiber reinforced plastic. The endplates made of titanium allow for enhanced bone growth, while the plastic/PEEK spacer element allows for improved load absorption and distribution. The spinal implant device, using titanium endplates and a PEEK spacer, provides excellent radiolucency thereby eliminating the need for X-ray markers either intra- or post-operation. The manufacturing method for the hybrid spinal implant device uses injection molding to insert or back injection mold the spacer between the two endplates.

Method of making a spacer device having a containment body
20170071745 · 2017-03-16 ·

A method of making a spacer device or a device to be implanted in a human body that includes a containment body and is suitable for treating a bone seat or a joint seat of the human body includes a base portion and side walls that extend from the base portion and that delimit between them at least one cavity, wherein the containment body has a plurality of pores and/or at least one opening, configured to place the at least one internal cavity in communication with the outside of the containment body.

IMPLANTABLE SYSTEMS, DEVICES AND RELATED METHODS

The present application is generally directed to implantable systems, devices and related methods pertaining to spinal surgery. In particular, the present application discloses a frame and spacer system for inserting into a disc space. The frame and spacer system is of low profile. The frame can receive different fixation devices, including threaded and non-threaded fixation devices.

IMPLANTABLE SYSTEMS, DEVICES AND RELATED METHODS

The present application is generally directed to implantable systems, devices and related methods pertaining to spinal surgery. In particular, the present application discloses a frame and spacer system for inserting into a disc space. The frame and spacer system is of low profile. The frame can receive different fixation devices, including threaded and non-threaded fixation devices.

DEVICES AND METHODS FOR BONE FIXATION
20250099265 · 2025-03-27 ·

Devices and methods for bone fixation including a bone fixation system including a bone plate or intervertebral spacer including a plurality of apertures dimensioned to receive bone fasteners and at least one polymeric element capable of transitioning from a solid state to a flowable state. The polymeric element transitions to a flowable state as a result of exposure to ultrasonic vibration. The polymeric element is placed on the bone plate or intervertebral spacer adjacent a fastener in an aperture and acts to prevent rotational and/or translational movement of the fastener relative to the bone plate or intervertebral spacer.

A flexible meniscus prosthesis

Provided herein is an arc-shaped meniscus prosthesis with a first end having a first fastening part for securing the first end to a bone surface and a second end having a second fastening part for securing the second end to a bone surface. A curved intermediate section connects the first end and the second end. The curved intermediate section is made of a single first biocompatible, non-resorbable material that has a tensile modulus of at most 160 MPa. The first material is isotropic with regard to the tensile modulus and the intermediate section is a monolithic piece of the first material.

Intervertebral implant

The intervertebral three-dimensional structure comprises a top side, an underside, a front face, a rear face, and a plurality of boreholes designed to receive affixation elements.