Disclosed is a fenestrated bone anchor suitable for being anchored in live bone tissue of a human or animal patient. The bone anchor comprises a shaft with a proximal end and a distal end and a circumferential surface extending from the proximal end to the distal end. The shaft further comprises a longitudinal cavity extending from the proximal end towards the distal end and a plurality of lateral channels extending through a wall of the shaft from the axial cavity to the circumferential surface. The lateral channel has a pear-shaped cross section and/or the thickness of the wall increases gradually in selected ones of directions towards the lateral channels. The fenestrated bone anchor is e.g. a component of a surgical system comprising an interbody fusion device of the stand-alone type.

A pivotal bone anchor assembly includes a shank having an anchor portion and a head with a partially spherical outer surface, a drive socket, an annular planar top surface surrounding the drive socket, and a frusto-conical surface between the planar top surface and the partially spherical outer surface. The assembly further includes a receiver having a base defining an axial bore and an upper portion defining a channel configured to receive a rod, and an insert positionable within the axial bore having an upper surface engageable with the rod, a lower surface for transferring a downwardly-directed force toward the head, and a central aperture for accessing the drive socket, with the rod extending across the central aperture when the fixation rod is engaged by the upper surface. After the head, the insert, and the rod are positioned in the receiver, the frusto-conical surface remains spaced apart from the rod to provide for increased articulation of the shank relative to the receiver.

The invention relates to a biodegradable, magnesium-containing bone screw for implanting into a patient body for use in medical applications, such as, orthopedic, craniofacial and cardiovascular surgery. The bone screw has a head, shaft and tip. The thickness of the head is greater than the thickness of conventional bone screws. The shaft includes both a non-threaded and a threaded portion. The tip is non-threaded and pointed, such as, conical in shape. The composition of the bone screws provide for improved biodegradability and biocompatibility, and the features of the structure of the bone screws facilitate guidance and placement during implantation as well as reduce the potential for mechanical failures.

A bone screw comprising a shaft having a wall, the wall including a minor diameter and at least one thread having an external thread form. The thread form including a first portion comprising a crest of the thread form and a second portion extends between a minor diameter of the thread form and the first portion. The first portion having a solid configuration relative to the second portion. In some embodiments, systems, spinal constructs, surgical instruments and methods are disclosed.

A compression device made of a superelastic material having a peripheral portion with an upper surface, a lower surface, and a central opening extending therethrough is provided. One or more resilient teeth project inward of the peripheral portion into the central opening and are configured to exert a biasing force in an axial direction when deformed in a direction opposite the axial direction.

This disclosure is directed to surgical fixation devices (e.g., staples, screws, etc.) which are able to bring bone fragments into close proximity with each other, generate a compressive load, and maintain that compressive load for a prolonged period of time while healing occurs. The surgical fixations devices are manufactured from a shape memory material (e.g., a material capable of exhibiting superelasticity and/or a temperature-induced shape change).

A bone screw includes a screw body having a head at one end of the screw and a tip at an opposite end of the screw; head threads directly attached to the screw body and continuous around the head of the screw; tip threads directly attached to the screw body and continuous around the tip of the screw; and overhanging thread portions between the head threads and the tip threads, the overhanging thread portions spaced apart, with unthreaded channels between the overhanging thread portions and the overhanging thread portions overhanging a portion of the unthreaded channels.

The present invention relates to implantable medical devices (dental and orthopedic) (osseointegrable implants) textured by the additive manufacturing process. Such implants are prepared in such a way as to comprise a larger surface area of contact between implant/adjacent tissues, porous microstructure with complex geometry with controlled and diversified pore size, which confers several technical advantages. In addition, the present invention relates to the process of preparing said implants and/or screws with an optimized structure for accelerating osseointegration. Finally, the present invention refers to the use of said implants as carriers of drugs or cells in order to treat the site, promote its healing, tissue regeneration or promote cell growth.

An intramedullary (IM) nail insertion assembly includes an IM nail extending longitudinally from a proximal end to a distal end. A proximal portion of the IM nail has an internal threading. The IM nail insertion assembly also includes a connecting screw extending longitudinally from a proximal end to a distal end. A distal portion of the connecting screw has an external threading for engaging the internal threading of the TM nail. One of the proximal portion of the IM nail and the distal portion of the connecting screw has a feature to resist a disengagement of the proximal portion from the distal portion.

A medical implant identification system is disclosed. The implant identification system may include a probe reader extending from a proximal end to a distal end and the distal end may include a faraday cage. The probe reader may be in communication with an operating room computer and/or a display. The implant identification system may include at least one digital set screw comprising an antenna disposed in an antenna portion of the digital set screw. In various embodiments, the faraday cage may have a size and shape corresponding to a size and shape of the antenna portion of the digital set screw. Additionally, the antenna may be configured to transmit identity information to the probe reader, and the identify information may be displayed by the display and/or stored in a data store of the operating room computer.