A multi-layer, fiber-reinforced composite orthopaedic fixation device having a design selected based on a desired characteristic of the orthopaedic fixation device. The design may be selected according to a model of the device, the model defining design constraints, and the design may comprise a pattern of the fiber angle for each layer. The selection of a design may be analyzed using finite element analysis to determine whether the design will comprise the desired characteristic.

A programmable medical wire system includes a programmable wire assembly that includes: a core conductor; at least one actuator conductor electrically coupled to the core conductor, the actuator conductor being programmed to move toward a predetermined shape based on actuation; at least one selective conductor electrically coupled to the actuator conductor and configured to be electrically energized to actuate the actuator conductor to move toward the predetermined shape; at least one emitter configured to produce electromagnetic radiation of a given wavelength coupled to the programmable wire assembly; and at least one detector configured to receive emissions of the emitter and communicate signals of the emission remotely from the emitter. One or more of the selective conductors can be energized to activate the actuator conductors and/or core conductor and cause the actuator conductors and/or core conductor to bend or twist in a preprogrammed manner and return to original shape when deenergized. When de-energized, the actuator conductor and/or core conductor can resume its natural shape.

Systems and methods for ultrasonically-assisted placement of orthopedic implants is described herein. An example method may comprise delivering ultrasonic energy to a surgical instrument such as a screw driver, Jamshidi needle, awl, probe, or tap that is in contact with the bone region targeted for removal and/or being prepared for implant placement. The method may further comprise delivering the ultrasonic energy via a probe passed through a cannulated surgical instrument and/or implant. An example system may comprise an ultrasonic generator coupled to a transducer, a probe or surgical instrument coupled to the transducer, a cannulated surgical instrument that allows passage of the probe, and a computing device configured to control the ultrasonic generator and take input from the user.

A medical instrument includes an insertion section main body extending along a longitudinal axis, a rotation supporter attached to the insertion section main body, a power transmission member rotatably supported by the rotation supporter and having a blade to which a fluid is supplied, external teeth arranged on an outer circumferential surface of the power transmission member in a circumferential direction, a tubular rotation member disposed outside the power transmission member in a radial direction, internal teeth arranged on an inner circumferential surface of the rotation member in the circumferential direction, and a fluid duct configured to supply the fluid to the blade. The power transmission member is configured to rotate by receiving power generated in the blade due to supply of the fluid. The rotation member is configured to rotate about the longitudinal axis by receiving the power from the power transmission member as the internal teeth are meshed with the external teeth.

A bidirectional thermally actuated component includes a heating element and wax material provided in an enclosed housing wherein the heating element is activated to melt the wax which expands to cause movement of the housing or an element mounted therein. When the heating element is deactivated, the was hardens and constricts to allow for movement in the opposite direction based on application of a force in the opposite direction, which may be provided by a biasing spring or a second actuator. An adjustable medical device may include the thermally actuated component to control adjustment of the device.

A battery-powered, modular surgical device comprising an electrically powered surgical instrument that requires a pre-determined minimum amount of electrical energy to complete a surgical procedure, and a power module assembly that has a battery that powers the surgical instrument and has a current state of electrical charge, and a control circuit that is electrically coupled to the battery and the surgical instrument and has a memory and a microprocessor. The microprocessor determines the current state of electrical charge of the battery, compares the current state of electrical charge to the pre-determined minimum amount of electrical energy, permits the battery to discharge if the current state of electrical charge is above the pre-determined minimum amount of electrical energy, and maintains the battery in a non-discharge state if the current state of electrical charge is below the pre-determined minimum amount of electrical energy.

A surgical stapling system is disclosed comprising a proximal housing portion, a distal housing portion removably coupleable to the proximal housing portion at a coupling interface, a motor, and a power source in electrical communication with the motor along an electrical communication pathway that does not traverse the coupling interface. The power source is configured to provide energy to the motor along the electrical communication pathway. The power source is permitted to provide energy to the motor based on the distal housing portion being coupled to the proximal housing portion.

Devices and methods for dermatology and more particularly to fluid enhanced skin treatment system for skin rejuvenation that can use an abrasive probe for removing epidermal layers while contemporaneously providing for the infusion of therapeutic fluids into the skin.

A portable and passive safety intraosseous device to allow for direct introduction of medications, etc., within the intermedullary space of a subject patient's bone or, if needed, the removal of certain substances from such a subject patient's bone. Such a device permits direct drilling and placement of a cannula within the subject bone with access external to the subject patient's skin, permitting, as well, connection of a tube for such introduction/removal purposes. The ability to provide a passive safety unit allows for facilitated utilization in, for instance, emergency situations with the entire device provided for utilization thereof. The device includes a drilling component with a permanently attached stylet and a removable cannula, a power supply for a single drilling operation, a mechanism to draw the stylet back into the drill component after use and disengagement from the cannula, and an automatic closure that activates with the separation of the cannula.

A detachable motor-powered surgical instrument. The instrument may include a housing that includes at least one engagement member for removably attaching the housing to an actuator arrangement. A motor is supported within the housing for supplying actuation motions to various portions of a surgical end effector coupled to the housing. The housing may include a contact arrangement that is configured to permit power to be supplied to the motor only when the housing is operably attached to the actuator arrangement.