A method of bone fixation includes placing a bone plate adjacent to a lesser trochanter on a medial aspect of a femur such that at least a portion of the lesser trochanter is positioned between appendages of the bone plate, wrapping cables coupled to the bone plate about a first and second bone fragment of a proximal femur, and tightening the cables to secure the first and second bone fragments together.

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.

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.

A smart medical device includes a structure configured to be at least partially implanted in a body, and an electronics cartridge that is configured to be inserted into the structure after the structure is implanted in the body. The structure may be a cannulated screw for use in treating bone fractures. The medical device includes an impedance sensor for monitoring and reporting on the healing state of bone fractures. The sensor includes components of the electronics cartridge and electrodes that are either associated with the cannulated screw or with the insertable electronics cartridge.

A retrograde intramedullary nail for insertion in the medullary canal of a femur includes a body that is elongate and defines a leading end and a trailing end spaced from each other at a length sufficient to extend from an intercondylar region at least to a subtrochanteric region of the femur. The body further defines a leading portion that extends to the leading end. The leading portion defines at least one locking hole configured to receive a fixation member. The at least one locking hole defines a central hole axis that is oriented to extend through the neck and head of the femur.

A fracture fixation system includes a bone nail configured to be inserted into a canal of a bone by insertion through a distal end of the bone, such that the first end of the bone nail is configured to be seated in a proximal end portion of the bone. The fixation system further includes a bone plate defining an inner surface and an outer surface. The inner surface of the bone plate is configured to abut a lateral surface adjacent the proximal end portion of the bone. The fixation system further includes a first bone screw configured to pass through a first opening defined by the bone plate and a first opening defined by a first portion of the bone nail adjacent the first end of the bone nail to secure the bone plate and the bone nail together.

Intramedullary nails, systems, and methods. The intramedullary nail may include a generally elongate body extending from a first, distal end to a second, proximal end. The distal end may include one or more openings configured to receive one or more bone anchors that extend transversely through the distal end intramedullary nail, and thereby configured to secure the distal end of the nail. The proximal end may also include one or more openings configured to receive one or more bone anchors that extend transversely through the proximal end of the intramedullary nail, and thereby configured to secure the proximal end of the nail. In some embodiments, the proximal opening may contain one or more relief cuts.

Intramedullary nails, systems, and methods. The intramedullary nail may include a generally elongate body extending from a first, distal end to a second, proximal end. The distal end may include one or more openings configured to receive one or more bone anchors that extend transversely through the distal end intramedullary nail, and thereby configured to secure the distal end of the nail. The proximal end may also include one or more openings configured to receive one or more bone anchors that extend transversely through the proximal end of the intramedullary nail, and thereby configured to secure the proximal end of the nail. In some embodiments, the proximal opening may contain one or more relief cuts.

The present invention relates to an improved orthopaedic device for athrodesis, in particular for the arthrodesis or fusion of a joint, for example an ankle joint, of the type comprising of a nail having head and tip ends opposed to each other; at least a first portion of the nail having an axis of symmetry; a single circular first transverse hole made in the first portion near the head of the nail and extended according to its own axis perpendicularly to the axis of symmetry; a slotted second transverse hole still made in the first portion of the nail and extended perpendicular to both the first axis of symmetry; and to the axis of the first transverse hole; and the slotted second transverse hole being made at a greater distance with respect to the head of the nail than the distance from the head of the first transverse hole.

The invention herein described is an endoprosthesis intended to replace a resected portion of bone and joint. The invention can be non-invasively, manually operated to lengthen a patient's limb both intraoperatively and postoperatively. It includes bone anchoring components for anchoring to a first and second long bone, a joint to replace the function of an orthopedic joint, and a purely mechanical lengthening mechanism which can be located and operated manually by an operator by pressing on skin of a patient without requiring a surgical incision. An alternative embodiment of the invention describes a similar extendable endoprosthesis which is unlocked by an operator by pressing on skin of a patient and the limb is subsequently pulled or pushed by the operator to change its length. The invention does not need or include any magnets, electric motors, electric current, application of heat or a fluid displacement (hydraulic) system.