A bone plate system and method for implanting the bone plate. The bone plate may include a head portion and a shaft portion, the shaft portion having a longitudinal axis and comprising a plurality of discrete aperture clusters. Each aperture cluster may include a non-threaded, non-locking bone fastener aperture configured to provide a polyaxial compressive construct and at least one threaded, locking bone fastener aperture. Once aligned with the bone, a first bone fastener is inserted into the bone through at least one of the non-threaded apertures in a direction normal to the longitudinal axis, compressing the bone along the longitudinal axis of the shaft portion of the bone plate. A second bone fastener is inserted into the bone through at least one of the threaded, locking bone fastener apertures in a direction oblique to the longitudinal axis and securing the bone plate to the bone.

A bone plate system and method for implanting the bone plate. The bone plate may include a head portion and a shaft portion, the shaft portion having a longitudinal axis and comprising a plurality of discrete aperture clusters. Each aperture cluster may include a non-threaded, non-locking bone fastener aperture configured to provide a polyaxial compressive construct and at least one threaded, locking bone fastener aperture. Once aligned with the bone, a first bone fastener is inserted into the bone through at least one of the non-threaded apertures in a direction normal to the longitudinal axis, compressing the bone along the longitudinal axis of the shaft portion of the bone plate. A second bone fastener is inserted into the bone through at least one of the threaded, locking bone fastener apertures in a direction oblique to the longitudinal axis and securing the bone plate to the bone.

A surgical instrument is separable into a transducer unit and a lower body portion. The lower body portion includes a waveguide and a casing. The transducer unit includes a transducer and a geared mechanism operable to couple the transducer to the waveguide. In some versions the geared mechanism includes bevel gears coupled to a rack and pinion such that linear motion may be used to rotatably couple a transducer to a waveguide. The rack gear may further include a handle extending out of the transducer unit casing to be actuatable by a user. The rack gear may also be flexible or rigid. In other versions, the bevel gears may be coupled to a threaded shaft that is operable to translate the transducer into the waveguide to form an interference fit. The transducer unit may also include a slide lock mechanism to couple to the casing of the lower body portion.

An apparatus includes an instrument body and transmission assembly. The instrument body includes a motor, a switch, and an energy source (e.g., an ultrasonic transducer). The transmission assembly includes an end effector, a transmission feature (e.g., an acoustic waveguide), and a switch engagement feature. The end effector includes an active feature (e.g., a harmonic blade) in communication with the energy source. The switch engagement feature is operable to mechanically couple the energy source with the transmission feature in response to the switch engagement feature triggering the switch. A yoke of the instrument body is configured to selectively engage a translating member of the transmission assembly. A release switch is operable to selectively disengage the yoke from the translating member.

In the cover for a blood pressure meter according to the invention, a coupling region that is detachably attached to a bottom surface of a main body is provided on one end. A tray region that is disposed so as to face a back surface of the main body and receives an accommodated cuff belt is connected to the coupling region. A panel cover region capable of covering a front panel of the main body is provided on the other end. A storage cover region that connects the tray region and the panel cover region is provided. In a cover-coupled state where the coupling region is detachably attached to the bottom surface of the main body, the panel cover region and the storage cover region are configured to be openable and closable with respect to the front panel and the tray region.

Containers and methods protect surgically-removed tissue such as cranial bone flaps for limited times during surgery. In some cases, tissue protected in such a container can be returned to the patient, lessening the need for synthetic, allographic, or xenographic alternatives. A container may include a frame defining a plurality of retention compartments, each retention compartment having an orientation and comprising sidewalls supported by the frame, wherein the sidewalls define a rim for each retention compartment in the plurality of retention compartments, wherein the orientation of a first retention compartment in the plurality of retention compartments differs from the orientation of a second retention compartment in the plurality of retention compartments.

A lid (100) for a container (1901) includes a first sliding door (102) and a second sliding door (103). A lid body (101) has a container engaging section (104) and an interior section (103) having a sliding surface (120) and a sharps disposal aperture (119). The second sliding door interlocks between the sliding surface and the first sliding door. The first sliding door and the second sliding door are selectively slidable between: an open position (1100) with a minor protuberance (124) and the major protuberance (125) disposed beneath the second sliding door; a partially closed position (1500) with an edge (701) of the second sliding door disposed between the minor protuberance and the major protuberance; and a closed position (1700) with the major protuberance disposed between the edge of the second sliding door and the minor protuberance.

A surgical instrument system and method are disclosed. The surgical instrument system includes an instrument case and a charging plate that may be placed in a sterile surgical field. The charging plate is configured to receive electrical power from outside the sterile surgical field and transmit that electrical power to other devices within the sterile field.

A container holds at least one surgical implement, has a lock mechanism, and has a signature label that impedes access to the surgical implement until the correct surgical site is confirmed. A method of using the container includes the steps of confirming the correct surgical site, signing the label and removing it from the container, placing the label in the medical record, unlocking the container, removing the implement, and beginning the surgery, wherein the surgical team is forced to pause to confirm the correct surgical site before starting the surgery. The system and method may also include a wrong site surgery profile used by individuals within the surgical procedure environment and third parties for tracking and determining if, and where, a wrong site surgical procedure occurred. The profile can be updated, tacked and monitored while a patient is interacting within the medical environment.

A container holds at least one surgical implement, has a lock mechanism, and has a signature label that impedes access to the surgical implement until the correct surgical site is confirmed. A method of using the container includes the steps of confirming the correct surgical site, signing the label and removing it from the container, placing the label in the medical record, unlocking the container, removing the implement, and beginning the surgery, wherein the surgical team is forced to pause to confirm the correct surgical site before starting the surgery. The system and method may also include a wrong site surgery profile used by individuals within the surgical procedure environment and third parties for tracking and determining if, and where, a wrong site surgical procedure occurred. The profile can be updated, tacked and monitored while a patient is interacting within the medical environment.