A tibial implant includes one or more stiffness-modifying features to reduce the stiffness of one or more sections of the tibial implant. The stiffness-modifying features may include slots, recesses, or passageways defined in various locations of the tibial implant to selectively reduce the stiffness of a tibial insert and/or tibial base of the tibial implant.

A flexible hip joint stem includes a shoulder body connecting piece, a flexible stem body, a stem tail, and a center regulating rod. The flexible stem body includes an inner-layer cylinder and an outer-layer cylinder. The inner-layer cylinder and the outer-layer cylinder are both composed of spiral springs, where the spring wire width of the spiral springs is basically equal to the screw pitch. The regulating rod passes through the shoulder body connecting piece and the flexible stem body, and is fixed with the stem tail by screwing the threads, which allows the inner-layer cylinder and the outer-layer cylinder to produce a certain degree of elastic deformation, limits the range of the elastic deformation, and enables the flexible hip joint stem to have sufficient supporting strength as a whole.

An artificial joint is provided. The artificial joint may comprise: a first joint member including a first bone replacement part, and a (1-1).sup.st branch and a (1-2).sup.st branch branched from opposite sides of the first bone replacement part; a second joint member including a second bone replacement part, and a (2-1).sup.nd branch and a (2-2).sup.nd branch branched from opposite sides of the second bone replacement part; a first main string connecting one side of the (1-1).sup.st branch and one side of the (2-1).sup.nd branch; a second main string connecting the one side of the (1-1).sup.st branch and one side of the (2-2).sup.nd branch; a third main string connecting one side of the (1-2).sup.st branch and the one side of the (2-1).sup.nd branch; and a fourth main string connecting the one side of the (1-2).sup.st branch and the one side of the (2-2).sup.nd branch.

A sleeve for use with a percutaneous, external fixation device is disclosed, wherein the sleeve includes a sleeve body with an interior space in which the percutaneous device can be disposed, a flange that extends at a substantially perpendicular angle to the sleeve body, and a cutting edge extending from the sleeve body below the flange. The cutting edge is designed for placement in contact with the skin adjacent to the percutaneous device so as to define a leading edge thereof in a primary anticipated direction of migration of the percutaneous device. Kits and assemblies that include sleeves and percutaneous devices are also disclosed. Further disclosed are methods of reducing tension in a patient's skin following placement of the percutaneous device via use of the sleeve, as well as methods of adjusting and readjusting the assembly upon placement.

A prosthetic disc can take the form of a sensing artificial disc that includes a resilient core and at least one sensor configured to sense one or more conditions within and/or experienced by the disc. The sensing artificial disc can serve as a replacement to a failed or injured disc between two vertebrae of a spine. The sensing artificial disc can include at least one element configured to change a condition or property of the resilient core in response to a condition sensed by the at least one sensor. A prosthetic disc can include therapeutic system configured to deliver medication to the body, which can include a reservoir of medication.

The present disclosure comprises a ball head, a neck part, a cover body, and a fastener, wherein the cover body is in a shape of a thin-walled cup, including a cup buckled and embedded on the femoral neck left after the femoral head is removed and a circle of skirt plates attached to the lower edge of the cup to extend the covering range of the cup to the femoral neck and the intertrochanteric femur; a through hole for a cable to penetrating through is formed in the tail end of each skirt plate, and a limiting clip for limiting the cable for cerclage of the cup is arranged outside the skirt plate; and then stable rigid connection is conducted using a compression ring; and the fastener comprises a screw or an additional perforated steel plate and a cable which is fixed in a cerclage and tension manner.

A system and method for sharing and absorbing energy between body parts. In one particular aspect, the system facilitates absorbing energy between members forming a joint such as between articulating bones.

A prosthetic disc can take the form of a sensing artificial disc that includes a resilient core and at least one sensor configured to sense one or more conditions within and/or experienced by the disc. The sensing artificial disc can serve as a replacement to a failed or injured disc between two vertebrae of a spine. The sensing artificial disc can include at least one element configured to change a condition or property of the resilient core in response to a condition sensed by the at least one sensor. A prosthetic disc can include therapeutic system configured to deliver medication to the body, which can include a reservoir of medication.

Proposed is a spinal cage. The spinal cage includes a bone support portion configured to be disposed between a first vertebra at an upper side and a second vertebra at a lower side to support the first vertebra, a base portion positioned at a lower side of the bone support portion to come in contact with the second vertebra, and a sidewall portion which has an upper side end connected to an edge of the bone support portion and a lower side end connected to an edge of the base portion and includes an elastic band having elasticity and inelastic bands having relatively lower elasticity or no elasticity. Therefore, subsidence of the spinal cage into vertebrae can be suppressed.

In some aspects, the present invention is a medical implant with an independent endplate structure that can stimulate bone or tissue growth in or around the implant. When used as a scaffold for bone growth, the inventive structure can increase the strength of new bone growth. The independent endplate structures generally include implants with endplates positioned on opposite sides of the implant and capable of movement independent of one another. In most examples, the endplates have a higher elastic modulus than that of the bulk of the implant to allow the use of an implant with a low elastic modulus, without risk of damage from the patient's bone.

A method of designing independent endplate implants is also disclosed, including ranges of elastic moduli for the endplates and bulk of the implant for given implant parameters. Implants with elastic moduli within the ranges disclosed herein can optimize the loading of new bone growth to provide increased bone strength.