An interbody implant can comprise a cage and a porous structure. The cage can comprise an anterior segment, a medial segment, a posterior segment and a lateral segment contiguously connected to each other to define an interior space. The porous structure can be located in the interior space and can be bounded by the cage. The porous structure can comprise opposed superior and inferior surfaces exposed through the cage, an internal cavity located in an interior of the porous structure, and a plurality of ports connecting the internal cavity to the superior and inferior surfaces. A superior-inferior stiffness of the interbody implant can be defined by the porous structure. The porous structure can be compressed within a patient by movement of the spine to biologically stimulate bone growth in vertebrae adjacent the interbody implant. The implant can be configured for lateral, anterior and posterior insertion at different spine levels.

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 a guide element, 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.

A bone fusion method, system and device for insertion between bones that are to be fused together and/or in place of one or more of the bones, such as, for example, the vertebrae of a spinal column. The bone fusion device comprises one or more extendable tabs having a central rib. The bone fusion device includes one or more support channels configured to receive an insertion instrument that is then secured to the bone fusion device via a coupling mechanism. As a result, the coupled device is able to be securely positioned between vertebrae using the insertion instrument with minimal risk of slippage.

An orthopaedic knee prosthesis includes a tibial insert and a femoral component configured to articulate on the tibial insert. The tibial insert includes a lateral articular surface and medial articular surface that is asymmetrically shaped relative to the lateral articular surface. The medial articular surface is shaped to reduce anterior translation of a medial condyle of the femoral component, while the lateral articular surface is shaped to allow a lateral condyle of the femoral component to pivot, relative to the medial articular surface, along an arcuate articular path. Additionally, one or both condyles of the femoral component may include a femoral articular surface having a curved femoral surface section defined by a continuously decreasing radius of curvature.

Expandable fusion devices, systems, and methods thereof. The expandable implant may include first and second lateral legs and link plates pivotably joined between them. The lateral legs may include upper and lower endplates configured to engage adjacent vertebrae, an actuator assembly including a rotatable actuator having a shaft and a rotatable nut, and driving ramps positioned along the shaft of the actuator. The actuator assembly may cause independent movement of one or more of the driving ramps, thereby causing an expansion in height of the upper and lower endplates of the lateral legs and passive expansion of the connected link plates.

Embodiments of an artificial meniscus implant are disclosed herein. An artificial meniscus includes at least one circumferential fiber and at least one non-circumferential fiber embedded within an arc-shaped body. The non-circumferential fibers may form loops extending through a peripheral edge of the implant, and the circumferential fibers may extend out of anterior and posterior horns of the implant to terminate in ends that are configured for fixation to bone. The ends may be interconnected, and covered by horn extensions to protect the ends from wear at the bone interface. Methods of making and implanting artificial meniscus are also disclosed herein. The method of making includes stepwise molding, layering, and curing of polymer material around the circumferential fibers and sewing the non-circumferential fibers into the polymer material. Methods of implanting may include threading ends of circumferential fibers through first and second bone tunnels.

Spinal interbody fusion implants for use in posterior lumbar interbody fusions (PLIF), anterior lumbar interbody fusions (ALIF), transforaminal lumbar interbody fusions (TLIF) and transpsoas interbody fusions (DLIF), each of the implants including a 3-D printed titanium frame having meshed sidewalls, open top and bottom faces and a selectively closeable back plate for enclosing a posterior end of the frame. A machined, acid treated allograft bone graft is contained within the frame, the bone graft having a window for containing a biomaterial, anti-migration teeth and a ridge configured to mate with a slot within the frame for locking the graft in the frame.

The disclosure provides a meniscus substitute and a knee joint prosthesis with the meniscus substitute. The meniscus substitute includes; a base body, disposed on a tibial plateau or a tibial plateau prosthesis of a tibia; a polymer joint body, disposed on the base body; and a bone screw, disposed in the tibia in a penetration manner and connected with the base body.

A method and apparatus can include: a delivery tool having an insertion mandrel; an implant having a distal segment coupled to a proximal segment, the proximal segment having a proximal segment upper and a proximal segment lower, the distal segment having a distal segment upper and a distal segment lower, the implant including: a straight configuration based on the insertion mandrel being extended through the proximal segment and the distal segment, and a curved configuration based on the insertion mandrel being retracted from the distal segment; and an expansion mandrel configured for insertion into the implant, the implant including an expanded configuration based on the expansion mandrel being inserted between the proximal segment upper and the proximal segment lower, and being inserted between the distal segment upper and the distal segment lower.

An artificial functional spinal unit including an expandable intervertebral implant that can be inserted via a posterior surgical approach and used with one or more facet replacement devices to provide an anatomically correct range of motion is described. Lordotic and non-lordotic expandable, articulating implants and cages are described, along with embodiments of facet replacement devices and instruments for insertion. Methods of insertion are also described.