A spinal interbody device includes a base link comprising a first end and a second end, the base link including a cutout extending through the base link between the first end and the second end; a linkage including a first link having a first end coupled to the first end of the base link and a second end, the first link including a first aperture extending through the first link and defining a first longitudinal axis; and a second link having a first end coupled to the second end of the first link and a second end coupled to the second end of the base link, the second link including a second aperture extending through the second link and defining a second longitudinal axis. The base link and the first and second links define top and bottom surfaces configured to engage adjacent portions of bone, and first and second sides extending between the top and bottom surfaces. When the linkage is movable relative to the base link between a collapsed position and an expanded position, wherein when in the expanded position, an unobstructed line of sight is provided through the cutout and the first aperture along the first longitudinal axis and through the cutout and the second aperture along the second longitudinal axis.

A spinal interbody device includes a base link comprising a first end and a second end, the base link including a cutout extending through the base link between the first end and the second end; a linkage including a first link having a first end coupled to the first end of the base link and a second end, the first link including a first aperture extending through the first link and defining a first longitudinal axis; and a second link having a first end coupled to the second end of the first link and a second end coupled to the second end of the base link, the second link including a second aperture extending through the second link and defining a second longitudinal axis. The base link and the first and second links define top and bottom surfaces configured to engage adjacent portions of bone, and first and second sides extending between the top and bottom surfaces. When the linkage is movable relative to the base link between a collapsed position and an expanded position, wherein when in the expanded position, an unobstructed line of sight is provided through the cutout and the first aperture along the first longitudinal axis and through the cutout and the second aperture along the second longitudinal axis.

A placeholder for vertebrae or vertebral discs includes a tubular body, which along its jacket surface has a plurality of breakthroughs or openings for over-growth with adjacent tissue. The placeholder includes at least a second tubular body provided with a plurality of breakthroughs and openings at least partially inside the first tubular body. The first and second tubular bodies can have different cross-sectional shapes, can be are arranged inside one another by press fit or force fit or can be connected to each other via connecting pins and arranged side by side to one another in the first body.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

An interbody implant and inserter tool for spinal fusion. The interbody implant includes a cage portion and a nose portion. In some embodiments, an outer surface of the nose portion defines at least a first concave profile in a first direction, and may define a second concave profile in a second direction, the second direction being perpendicular to the first direction. The outer surface may also define an oblong cross-section normal to a nose axis. The oblong cross-section may be axisymmetric or continuously curved (or both) about the nose axis. The concave profile(s) enable easier initial insertion of for more precisely locating the interbody implant, so that the greater insertion forces required during implantation do not occur until the interbody implant is securely and accurately placed.

The invention relates to resorbable crosslinked form stable membrane which comprises a composite layer of collagen material and inorganic ceramic particles containing 1.5 to 3.5 weight parts of inorganic ceramic for 1 weight part of collagen material, sandwiched between two layers of elastic pretensed collagen material (collagen material that has been stretched such as to be in the linear/elastic region of the stress-strain curve), the collagen material comprising 50-100% (w/w) collagen and 0-50% (w/w) elastin, and has shape and dimensions suitable for use in human tissue regeneration outside the oral cavity in rhinoplasty, postlateral spinal fusion or orbital reconstruction.

Embodiments of the present invention are directed to microscale and millimeter scale tissue scaffolding structures that may be static or expandable and which may be formed of biocompatible metals or other materials that may be coated to become biocompatible. Scaffold structures may include features for holding desired biological or physiological materials to enhance selected tissue growth. Scaffolding devices may be formed by multi-layer, multi-material electrochemical fabrication methods.

The bionic dislocation-proof artificial lumbar vertebrae and disc complex comprises vertebral body components, intervertebral disc components and screws; the vertebral body components comprise an oval column; the intervertebral disc components comprise L-shaped arc plates and composite pads, the L-shaped arc plates comprise bottom plates, lateral plate and the raised column; end of the raised column is the ball shell with two raised arc; the composite pad is connected to the groove on the oval column; the ball shell and the composite ball form the ball and socket joint. The present invention replaces the removed vertebrae and adjacent discs and maintains the rotation, flexion and extension and buffer function, which ensures the stability and mobility of the lumbar spine after surgery. The present invention better resembles the normal physiology.

A laterally deflectable asymmetric implant for implanting into a body may comprise a deflectable piece having distal and proximal ends and assuming a straightened insertion state. The backbone may abut or interconnect with said deflectable piece at the distal end of the deflectable piece. In a fully deflected state the implant may define an asymmetric shape, e.g. a D-shaped loop, defining an at least partially enclosed volume. The deflectable piece may comprise a sequence of segments interconnected at effective hinges. Longitudinal pressure applied to the proximal end of the deflectable piece (or applied to the backbone in an opposite direction) may cause relative longitudinal movement between the backbone and the proximal end of the deflectable piece and may generate outward horizontal movement of the deflectable piece away from the backbone. In one embodiment, the implant is implanted using lateral access into an anterior zone of a vertebra and deployed posteriorly.

An interbody implant and inserter tool for spinal fusion. The interbody implant includes a cage portion and a nose portion. In some embodiments, an outer surface of the nose portion defines at least a first concave profile in a first direction, and may define a second concave profile in a second direction, the second direction being perpendicular to the first direction. The outer surface may also define an oblong cross-section normal to a nose axis. The oblong cross-section may be axisymmetric or continuously curved (or both) about the nose axis. The concave profile(s) enable easier initial insertion of for more precisely locating the interbody implant, so that the greater insertion forces required during implantation do not occur until the interbody implant is securely and accurately placed.