A system and method for improving limb function through the use of percutaneous mechanical and neural interfaces. The system generally uses a hollow long bone axial rod that is inserted into the long bone medullary cavity. A transfer rod with a central channel is mounted to the long bone axial rod. An exterior body attachment is connected to the transfer rod and attachment rings attach muscle groups, fascia layers and dermal layers to the transfer rod. Additionally, the system is configured to collect and transmit nerve signaling data to an external processor and additionally configured to transmit data from the external processor to the plurality of nerves.

A medical instrument is provided and includes a housing and a shaft coupled to the housing. The shaft has a proximal end and a distal end. An end-effector assembly is disposed at the distal end of the shaft. The end-effector assembly includes first and second jaw members. At least one of the first and second jaw members is movable from a first position wherein the first and second jaw members are disposed in spaced relation relative to one another to at least a second position closer to one another wherein the first and second jaw members cooperate to grasp tissue therebetween. The medical instrument also includes one or more light-emitting elements and one or more light-detecting elements configured to generate one or more signals indicative of tissue florescence. The one or more light-emitting elements are adapted to deliver light energy to tissue grasped between the first and second jaw members.

Systems and methods for estimating anatomic alignment between two or more bones are described herein. An example method can include registering an anatomic reference frame. Additionally, the method can include establishing a respective rotational relationship between each of one or more bones and an orientation sensor attached to each of the one or more bones. The method can also include receiving, from each of the orientation sensors, orientation information, and then calculating an orientation of a bone relative to the anatomic reference frame. The method can further include calculating, using the respective orientations of the bones relative to the anatomic reference frame, an anatomic alignment parameter between first and second bones.

Disclosed is a sensor measuring patient spine vertebra angular orientation, including: a fastener, adapted to be fastened on a specific patient spine vertebra in a unique orientation relative to the specific vertebra, a support, solidary with the fastener in a unique orientation relative to the fastener, a detector, removably secured to the support in a unique orientation relative to the support and adapted to measure one or more parameters representative of the patient spine vertebra angular orientation.

A system and method for improving limb function through the use of percutaneous mechanical and neural interfaces. The system generally uses a hollow long bone axial rod that is inserted into the long bone medullary cavity. A transfer rod with a central channel is mounted to the long bone axial rod. An exterior body attachment is connected to the transfer rod and attachment rings attach muscle groups, fascia layers and dermal layers to the transfer rod. Additionally, the system is configured to collect and transmit nerve signaling data to an external processor and additionally configured to transmit data from the external processor to the plurality of nerves.

A bow shaped pulse meter for new-born patients, comprising a control unit (21) arranged in a central portion (3) of the pulse meter (1), a first arm (2) with an integrated first electrode and a second arm (2) with an integrated second electrode extending respectively in a bow from opposite sides of said central portion (3), said integrated electrodes are configured to be in contact with a patient body (not shown) when in use, said electrodes being further electrically connected to said control unit (21). The pulse meter being distinctive in that said first and second arm (2) and the control unit (21) comprising an integral core element (1a) being made of a material having flexible properties to allow the respective arms (2) to bend away from each other when the pulse meter (1) is being arranged into an applying or removing position on the patient's body, said material having further spring back properties so that the arms (2) naturally contract inwards such that said electrodes are maintained in contact with the patient's body when the pulse meter (1) is in the applied position, said pulse meter (1) further comprising a second layer (15) overmolding at least a portion of each arm of core element (1a), said material of the said second layer (15) being electro conductive forming the electrical connection between the electrodes and the control unit (21).

A delivery system for an intracorporeal device includes a sheath defining one or more lumens shaped to receive a delivery catheter or shaft and a guidewire. The system may include a delivery shaft having a distal coupling feature adapted to releasably couple with a proximal coupling feature of the intracorporeal device. The delivery system may further include a hub through which the delivery shaft and guidewire are passed. The delivery shaft may be coupled to a feature, such as a knob, that enables manipulation of the delivery shaft to decouple the distal fixation feature from the proximal fixation feature of the intracorporeal device in order to deploy the intracorporeal device within a patient.

Described herein are systems, devices, and methods for treating and/or monitoring a patient with a prematurely dilated cervix during pregnancy or a patient with a history of a prematurely dilated cervix in a previous pregnancy. The systems, devices, and methods described herein further provide monitoring of the status of a cervix by, for example, sensing a change associated with the cervix of a patient. The systems, devices, and methods described herein are configured to either partially or completely encircle the cervix of a patient and constrict the encircled cervix. In some embodiments, the systems, devices, and methods described herein comprise a first and a second coupler that reversibly couple together so that these embodiments are configured to be manually placed (i.e. the couplers are coupled together) and then either removed or adjusted by a healthcare provider (i.e. the couplers are decoupled from each other).

A subcutaneously implantable device includes a housing, a clip attached to the housing, and an electrode. The clip is configured to move between an open position and a closed position to increase or decrease an opening between the housing and the clip to anchor the device to a muscle, a bone, and/or a first tissue. The electrode is configured to contact an organ, a nerve, the first tissue, and/or a second tissue. Circuitry in the housing is in electrical communication with the electrode and is configured to provide monitoring, therapeutic, and/or diagnostic capabilities with respect to the organ, the nerve, the first tissue, and/or the second tissue.

Stimulation and recording electrode assemblies that are particularly useful for Automatic Period Stimulation (APS). Such embodiments are compatible with nerve monitoring systems to provide continuous stimulation of a nerve during surgery. Certain embodiments include an electrode assembly having cuff including a body and two ears extending from the body. Within the body, at least one electrode is supported and connected to a lead wire assembly. The ears can be brought together to enlarge a gap in the body so that the electrode assembly can be fixated around a nerve. Other embodiments include an electrode assembly including first and second needle electrodes that each have a tip. A body is provided to interconnect the needle electrodes and can be manipulated to move the tips either toward or away from one another. Disclosed embodiments provide nerve monitoring and stimulation in cases where the nerve is only partially dissected.