A system and method for improving upon an ability of a surgeon to repair traumatic bone injury using new materials, components, and structures. A structure may be used as an implant or a component of an external fixator for a fractured long bone with that structure having anisotropic and viscoelastic properties, such as through additive manufacturing techniques.

A hip implant is provided that includes a metal acetabular cup to be inserted into an acetabulum of the pelvis, a femoral head and neck portion with a polymer femoral head molded onto a metal formal head base that is attached to a metal femoral neck rod configured to be inserted into the neck of a femur, and a metal main body shaft configured to be inserted into a femoral shaft region of the femur and secured by bone screws. The head base may have stabilizing features, such as dimples and peripheral mounds, over which the femoral head is molded. The main body shaft also has diagonal hole located at the center line of the neck of the femur to receive the femoral neck rod at an adjustable angle. The femoral head interfaces with the acetabular cup as a smooth plastic-to-metal spherical-surface joint.

A prosthetic stem is configured to reduce the perioperative and intraoperative risk of catastrophic medical complications and death that may be caused by BCIS. The prosthetic stem includes one or more internal channels that are configured to self-regulate intramedullary pressure within a prepared bone channel as the stem is inserted into the channel, thus reducing the likelihood of BCIS without sacrificing biomechanics and maintaining a reliable and repeatable implantation process. The stem includes a head and a body, wherein the head is configured to serve as a joint replacement and the body is configured for insertion into the prepared bone channel of a patient. One or more internal channels in the stem are configured to control the pressure within the prepared bone channel during insertion of the stem into the channel, particularly by forming a path through which excess cement may flow as the stem proceeds into the prepared bone channel. By so limiting pressurization of cement during this process, the risk of BCIS complications and other potential harmful effects are reduced while still maintaining sufficient fixation of the prosthetic stem in the prepared bone channel.

A dampening device that can be coupled to a medical implant to eliminate harmful electrical oscillations. The device includes circuity that detects harmful electrical oscillations in the implant. The device also includes circuity that generates cancelling electrical signals that counter the detected electrical oscillations. Alternatively, in a medical implant having a taper junction such as a standard hip implant, resistance welding of the taper junction just prior to surgical implanting may be performed after the appropriately dimensioned components are selected to eliminate a metal on metal interface where corrosion is most likely to occur.

Apparatus (20) for performing a joint replacement procedure comprising: a vibrator (50) configured to be coupled to a stem (120) and be excited stem out from the canal.

The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

A trial neck for hip surgery and a method of attaching a trial neck to a bone canal preparation instrument. The trial neck includes a body portion having a bore for receiving a proximal end of the bone canal preparation instrument. The trial neck also includes an elongate neck part comprising a pair of arms extending from the body portion. The trial neck further includes a clamping mechanism comprising a live spring formed by the body portion and said pair of arms of the elongate neck part and an actuator, for moving the clamping mechanism between a clamping configuration and a non-clamping configuration. In the clamping configuration, the pair of arms of the elongate neck part are pinched together to cause an inner wall of the bore to urge against the bone canal preparation instrument to retain the proximal end of the bone canal preparation instrument within the bore.

A medullary rod has a peripheral wall defining the outer shape of the medullary rod, and inwardly delimiting a hollow space. The medullary rod also has a plurality of first partitions. The first partitions are generally parallel to one another, extend between the inner side of the medullary rod located along the inner edge of the long bone after implantation, and the outer side of the medullary rod located along the outer edge of the long bone after implantation. Each of the first partitions is integral with the peripheral wall at these inner and outer sides of the medullary rod.

A biological tissue rootage face (30) capable of closely bonding to a biological tissue (H, S) is composed of a biocompatible material and has numerous fingertip-shaped microvilli (41). The microvilli (41) have tip diameters in the order of nanometers. An implant (1) has the biological tissue rootage face (30) on a surface (11, 24) configured to root into a biological tissue (H, S). In a method for forming the biological tissue rootage face (30), a surface of a biocompatible material is subjected to laser nonthermal processing carried out by emitting a laser beam in air, to form numerous fingertip-shaped microvilli (41). The laser beam is a laser beam of an ultrashort pulse laser.

A system and method for improving mechanical assemblies, such as prosthetic implants, intended to be installed in living tissue such as bone. Force-imparting devices are adapted and may include angularity, which may be introduced with specialized additive manufacturing, which may impart congruent cross-sections while providing variable stiffness. In some cases, the variable stiffness may be “stretchy” in a longitudinal direction and “rigid” in a radial directional which may provide an assembly bias. Additive manufacturing may allow the material of a prosthesis to be varied (e.g., density/porosity) to create variable stiffness over a length.