An intervertebral implant may include a shaft having a proximal end, a distal end, a longitudinal axis, a minor diameter, and a helical thread disposed about the shaft along the longitudinal axis between the proximal end and the distal end of the shaft. The helical thread may include a major diameter and a concave undercut surface angled towards one of the proximal end and the distal end of the shaft. The intervertebral implant may be implanted within an intervertebral space between a superior vertebral body and an inferior vertebral body. A ratio of the major diameter to the minor diameter may be less than 1.50. The concave undercut surface may engage the superior vertebral body and the inferior vertebral body and may be shaped to resist at least one force transmitted between the superior vertebral body and the inferior vertebral body to stabilize the intervertebral space.

An interbody implant system for use in the spine includes a base comprising two or more bone contacting surfaces, at least one recess in at least one of the two or more bone contacting surfaces, the recess configured for containing a tooth, a deployable tooth to provide fixation between the base and the anatomy of a subject, a break-away bridge between the tooth and the base for providing a first relative position between the tooth and the base, and a locking mechanism for providing a second relative position between the tooth and the base.

A bone disunion fastener may include a fastener shaft, a helical thread, and a bone staple. The helical thread may include a concave undercut surface oriented towards one end of the fastener shaft. The bone staple may include a first bone-engaging feature, a second bone-engaging feature, and a middle portion with an opening. The bone disunion fastener may be implanted along a disunion between a first bone portion and a second bone portion. The concave undercut surface may be shaped to resist at least one force transmitted between the first bone portion and the second bone portion to stabilize the disunion. The first bone-engaging feature may engage the first bone portion and the second bone-engaging feature may engage the second bone portion to couple the bone staple to the bone portions and resist at least one force transmitted between the bone portions to stabilize the disunion.

The present invention relates to an implantable anterior cervical plate having a stackable superior design, which deflects soft tissue.

A plate and cage assembly for stabilization of vertebral bodies. The assembly includes at least one fixation member, a cage having a proximal wall, a superior surface and an inferior surface (the superior surface and the inferior surface for engaging adjacent vertebrae), and a plate coupled to the cage and having at least one hole traversing the plate at an angle for insertion of the at least one fixation member into one of the vertebral bodies. The proximal wall of the cage has a blind hole, and the plate has a threaded screw hole aligned with the blind hole in the proximal wall of the cage.

An orthopedic implant which generally includes a frame structure and a porous structure. Both the frame and porous structure at least partially define at least six surfaces which make a three-dimensional profile of the implant. The porous structure is positioned at least partially within the three-dimensional profile.

A system and method for altering bone growth on and within an orthopedic implant that includes an implant body; a plurality of electrodes, wherein each electrode is at least partially embedded in the implant body, and comprises: a set of primary electrodes comprising at least one electrode, wherein a non-embedded segment of each primary electrode is proximal to a bone growth region, a set of secondary electrodes comprising at least one electrode, wherein a non-embedded segment of each secondary electrode is distal to the bone growth region, and wherein the plurality of electrodes are configured to function in a stimulation operating mode, such that a subset of primary electrodes function as cathodes and a subset of secondary electrodes function as anodes; a control system comprising a processor, and circuitry that connects to the plurality of electrodes; and a power system.

A nuclear disc implant includes an inner fillable enclosure and an outer fillable enclosure. After insertion into a enucleated disc cavity, the inner enclosure is filled with a fluid and the outer fillable enclosure is filled with a curable material. The curable material is allowed to cure and the fluid is removed from the inner enclosure to leave an inner enclosure surrounded by an cured outer enclosure. A reinforcing band may be provided around the nuclear disc implant. An inflation tool to fill the nuclear disc implant is provided.

An intervertebral fusion device comprises a superior component, an inferior component, and a core component. The superior and inferior components are received between first and second vertebrae whereby a superior component top side of the superior component abuts against the first vertebra, and an inferior component bottom side of the inferior component abuts against the second vertebra. The core component is inserted between the superior and inferior components to determine a height of the intervertebral fusion device. First and second core profiles of the core component cooperate respectively with a first component profile of the superior component and a second component profile of the inferior component during insertion of the core component to guide the core component relative to the superior and inferior components. First and second core formations of the core component inter-engage respectively with a first component formation of the inferior component and a second component formation of the superior component to present a barrier to separation of the core component, the inferior component, and the superior component. A height of the intervertebral fusion device decreases in a coronal direction from a first lateral side to a second lateral side of the intervertebral fusion device.

A multi-member prosthesis including first and second elongated members and a central member, said multi-member prosthesis adapted to be advanced into a pilot SI joint opening in said dysfunctional SI joint via a posterior approach, the pilot SI joint opening comprising a sacrum opening and an ilium opening and a sacrum opening. The first elongated member adapted to be press-fit into the sacrum opening and the second elongated member adapted to be press-fit into the ilium opening. The central member including first and second elongated member securing means adapted to secure the first and second elongated members thereto.