A hip/shoulder prosthesis includes: a head component; a metaphyseal component; a diaphyseal nail, and a locking device. The head component includes: a front face and rear face; with a bore, and first and second shaped recesses in the rear face. The metaphyseal component includes: a central transverse aperture at an angle to the metaphyseal component's axis; a first end configured for threaded engagement within the bore of the head component; and a longitudinal hole that begins at the second end, transects the transverse aperture and reaches the first end, to receive the locking device. The diaphyseal nail is inserted in the femoral or humeral canal, and includes: fastening apertures that receive corresponding screws for fastening the diaphyseal nail to the femur or humerus; a portion configured to be received within, and engage, the transverse aperture of the metaphyseal component, and a transverse hole configured to receive the locking device.

An adjustable trial for spinal implant sizing. The trial has a first and second plate that is adjustable between zero and degrees by use of continuously sloped edges that interface with a positioning band having reciprocal sloped edges. Protrusions are attached to each plate and the positioning band, the rotation of which is used to change the angle of the plates. A tool used to rotate the protrusions is marked with the angle of movement.

An implant is disclosed. The implant has a first endplate, a second endplate, a base disposed between the first endplate and the second endplate, a plurality of adjustment arms operably connecting the base with the first endplate and the second endplate, and a plurality of pins disposed on at least one of the first endplate and the second endplate. The plurality of pins have different lengths. The plurality of adjustment arms are rotatably connected to a plurality of hubs that are axially slidable on at least some of the plurality of pins.

A spine implant (e.g., for a TLIF surgical procedure) is configured to be steered into place during implantation in conjunction with a complementary insertion instrument. The cage of the implant is constrained to a limited range of rotation about a post carried by the cage. The insertion instrument is configured to hold the post while controllably rotating the cage relative to the post in order to angularly position the implant during implantation. Range of rotational motion is controlled by the configuration of a groove in the post. A retaining pin of the implant extends from the cage into the groove of the post to rotationally connect the cage to the post.

An implant may include a body having a leading edge portion, a trailing edge portion, and an intermediate portion. The leading edge portion may include a substantially smooth surface forming a substantial majority of a leading edge surface and the trailing edge portion may include a monolithic structure including at least one receptacle configured to receive an insertion tool. The intermediate portion may include a plurality of elongate curved structural members continuously formed with at least one of the leading edge portion and the trailing edge portion. In addition, the elongate curved structural members may be configured such that the intermediate portion remains substantially rigid under compressive forces during insertion of the implant between bone surfaces of a patient. Also, the elongate curved structural members may include an elongate curved structural member extending longitudinally from the leading edge portion to the trailing edge portion and having a substantially sinusoidal configuration.

The invention relates to a glenoid (shoulder socket) implant prosthesis, a humeral implant prosthesis, devices for implanting glenoid and humeral implant prostheses, and less invasive methods of their use for the treatment of an injured or damaged shoulder.

An expandable intervertebral fusion implant, including an inferior component, including a first top surface, a first bottom surface, a first end, a second end, and a first hole including a first portion and a second portion, a superior component, including a second top surface, a second bottom surface, a third end, and a fourth end, and an expansion mechanism including a flexible shaft arranged in the first hole, the flexible shaft including a fifth end, a sixth end connected to the first bottom surface, and a first plurality of teeth.

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 apparatus including a joint spacer for treatment of a joint of a human subject. The joint spacer includes a bioresorbable stent having compressed and expanded configurations and a covering that covers an external surface of the stent. The joint spacer is configured to be inserted into a space of the joint, and is shaped, when the bioresorbable stent is in the expanded configuration, to provide mechanical support to the joint until the bioresorbable stent resorbs into a body of the subject. Treating a joint of a human subject includes inserting a joint spacer into a space of the joint while a bioresorbable stent of the joint spacer is in a compressed configuration, and transitioning the bioresorbable stent to an expanded configuration within the joint, such that the joint spacer provides mechanical support to the joint until the bioresorbable stent resorbs into a body of the subject.

The invention discloses a bionic artificial hip joint. The artificial hip joint includes a femoral stem located above corpus femoris, and a convex force-bearing part is provided on the femoral stem. The force-bearing part abuts against the inner side of the cortex on greater trochanter and bears a part of the longitudinal stress; its hollow design is convenient for bone grafting, so that the prosthesis and the greater trochanter can be integrated. Replacement surgery can preserve the hard cortex on the greater trochanter, providing another focus point for the femoral stem and further improving the stability of the connection between the bionic artificial hip joint and corpus femoris.