A device, having a housing; a power source configured to supply electrical power to a conductive percutaneous implant in a circuit including the conductive percutaneous implant and tissue of a patient adjacent to the conductive percutaneous implant; an electrical sensor configured to generate a signal indicative of at least one electrical parameter of the circuit; and at least one data processing system having one or more processors configured to receive the signal and analyze the signal to determine at least one of a presence or change of infection of the tissue, and pass a control signal to the power source to vary the electrical power responsive to determining at least one of the presence or change of infection of the tissue.

Tension isolating adjustable adapters are disclosed, along with kits and systems containing same, as well as methods of production and use thereof. The tension isolating adjustable adapters include a percutaneous device holder that can be releasably connected to a percutaneous device via a locking element, and a tensioning member that engages the percutaneous device holder. The tensioning member has at least one tension pad that is shaped and configured to be disposed about the percutaneous device insertion site in the patient's skin, and the engagement of the tensioning member(s) to the percutaneous device holder allows for adjustment of the tension pad(s).

Tension isolating adjustable adapters are disclosed, along with kits and systems containing same, as well as methods of production and use thereof. The tension isolating adjustable adapters include a percutaneous device holder that can be releasably connected to a percutaneous device via a locking element, and a tensioning member that engages the percutaneous device holder. The tensioning member has at least one tension pad that is shaped and configured to be disposed about the percutaneous device insertion site in the patient's skin, and the engagement of the tensioning member(s) to the percutaneous device holder allows for adjustment of the tension pad(s).

An orthopaedic fixation assembly for prosthetic biologic attachment. The orthopaedic fixation assembly may include a main body with a longitudinally-extending stem having a proximal end, a distal end, and a cavity body. An anchor plug may be configured to be received within the stem cavity, and securable thereto via complementary mating surfaces. A spindle structure may be fixedly attached to the proximal end of the longitudinally-extending stem and protrude outwardly therefrom such that a portion of the structure extends externally beyond the resected cavity of the bone that may prevent rotational motion of the spindle. The spindle structure may have at least one compliant biasing member configured to apply a compressive force to the surrounding bone. A porous coating may be at the juncture between stem and spindle structure, on the spindle, and the splines and anti-rotation chocks, improving the initial stability of the implant and facilitating long-term bone ingrowth.

Methods and devices for approximating jaw and corresponding tissue segments are disclosed herein. In some embodiments, the approximation device includes a first jaw attachable to a first jaw segment, a second jaw attachable to a second jaw segment, the second jaw segment being smaller than the first jaw segment, and a housing. The second jaw is movably attached to the housing, the second jaw configured to move the second jaw segment toward the first jaw segment. The second jaw is configured to translate between a first position and a second position during a first segment of travel of the second jaw, and configured to at least rotate between the second position and a third position during a second segment of travel.

The present disclosure relates to external fixation struts and systems utilizing the external fixation struts. The struts include an elongated body comprising a first and a second hollow tubular shaft and include opposite connectors respectively coupled to an end portion of the first or the second shaft and each including a ball and socket joint. One shaft may have an internal diameter that is slightly larger than the external diameter than the other shaft to host internally the other shaft in a slidably and telescopic manner. A clamp element may provide a fast gripping action stopping the telescopic sliding of one shaft inside the other shaft. Each ball and socket joint connector may be structured to allow an angular movement of the corresponding connector with a spherical angle up to at least 90°.

A medical apparatus having a bar, the bar having a slot extending laterally along the bar; and a plurality of hooks, wherein the bar is an arch bar that is configured to be attached to a mandible or a maxilla. Such medical apparatuses may also have a plurality of arch bar fasteners, wherein each arch bar fastener is a bone screw having a threaded shaft and a compound head, the compound head having a threaded bore configured to receive a set screw. The medical apparatus may be used in methods to fixate a maxillary or mandibulary arch, or to aid in reducing a fracture of the mandible or maxilla.

An external fixation strut includes an elongated body including first and second tubular shafts. Opposite connectors are respectively coupled to one of the shafts and include a ball and socket joint. One shaft has an internal diameter slightly larger than the external diameter of the other to host the other shaft in a slidably and telescopic manner. The shafts of the strut are a synthetic radiolucent plastic material. A clamp element is in proximity of overlapping ends of the shafts for fast gripping action stopping the sliding of one shaft inside the other. A fixation element is manually operated and acts on the clamp element. A sleeve is provided around the central portion of the strut where the shafts overlap. The clamp element is a clamp band around the sleeve and includes opposite and facing gripping portions. The gripping portions are connected by a threaded connector of the fixation element.

A polyaxial bone anchoring device includes a receiving part with a rod receiving portion defining a recess for receiving a rod, and a head receiving portion with a wall that defines an accommodation space for accommodating a head of an anchoring element, and a locking member positionable at least partially around the head receiving portion and movable from a first position where the head can pivot in the accommodation space to a second position where an angular position of the head is locked. The wall of the head receiving portion further defines at least one cavity in communication with the accommodation space that reduces a radial thickness of at least part of the wall located between the accommodation space and the locking member, and at least part of the cavity is separated radially from the accommodation space by a portion of the wall.

A method of performing bunion surgery may involve attaching a bone positioning device to a first metatarsal and to a first cuneiform across a joint separating the first metatarsal from the first cuneiform. Attaching the bone positioning device can include inserting a first fixation pin into one of the first metatarsal or the first cuneiform and inserting a second fixation pin into an other of the first metatarsal or the first cuneiform. The method can involve using the bone positioning device to adjust an alignment of the first metatarsal relative to the first cuneiform; and, after adjusting the alignment of the first metatarsal relative to the first cuneiform using the bone positioning device, fixing a position of the first metatarsal relative to the first cuneiform with a bone connector.