Abstract: A pull wire can be retracted from a catheter by using a retraction system having an opening sized to pass through the pull wire and engage the catheter, two clamps positioned around the pull wire, a shuttle on which the clamps are mounted, and a slider having at least one contact for contacting and moving one or both clamps. To retract the pull wire, the slider can be moved proximally, the contact(s) can engage one or both clamps on the shuttle, the clamps can move so that the clamps come together and grip the pull wire, and the slider can then be moved further proximally to translate the shuttle, clamps, and pull wire proximally thereby extracting the pull wire from the catheter. The shuttle and slider can subsequently be moved distally without translating the pull wire.

Abstract: Implants can be used as flow diverters for treating aneurysms. Implants can include a stabilizing frame for anchoring the implant and an occluding element for diverting blood flow from the aneurysm neck. The stabilizing frame can have two parts, the first part sized to anchor within the sac of the aneurysm and the exterior part sized to anchor against a region of the blood vessel wall adjacent the aneurysm neck. The occluding element can be attached to the interior frame and positioned to occlude the aneurysm neck. The implant can have a central node that can be positioned near the center of the aneurysm neck at which the interior frame is attached to the exterior frame and from which the interior frame and the exterior frame extend.

Abstract: A number of low-profile metallic customized, patient-specific orthopaedic surgical instruments are disclosed.

Abstract: A sternal closure system for closing an opening in a sternum includes an implant and a plate pair comprised of first and second plates. The first and second plates secure with the sternum across the opening. The implant, in an insertion shape, inserts through the first and second plates and into the sternum across the opening, and then, upon a movement toward a natural shape, holds the opening closed while interconnecting the first and second plates. The sternal closure system alternatively includes an implant with a bridge having first and second apertures and first and second legs extending from the bridge. The implant, in an insertion shape, inserts into the sternum across the opening, and then, upon a movement toward a natural shape, holds the opening in the sternum closed. The implant, at the first and second apertures, receives fixation devices therethrough that engage the sternum.

Abstract: An articulating driver having a ball-in-socket joint. The driver may include a driver tip having a spherical head, a retention cap having a domed surface to mate with the spherical head, an input shaft, a spring disposed in an end of the input shaft and in a recess of the retention cap opposite that of the domed surface, and a housing that receives the input shaft, the spring, the retention cap and the spherical head. The housing may have a tapered end to positionally retain the spherical head therein. In another aspect, the driver may include a driver tip coupled to the input shaft that includes an interface to engage a screw. A bushing may engage the driver tip at one end and receive the screw at the other end to retain the screw within the driver.

Abstract: The disclosed technology can include a catheter braid including wire segments with varying cross-section shapes. Wire segments at a proximal portion of the braid can have a substantially rectangular cross-section shape, while wire segments at a distal portion of the braid can have a substantially circular cross-section shape. The cross-section shape can gradually transition from rectangular to circular along the length of the braid. The catheter braid can include wire segments having an outer core and an inner core. The inner core at the proximal section of the braid can have a substantially rectangular cross-section shape, while the inner core at the distal portion of the braid can have a substantially circular cross-section shape. The cross-section shape of the inner core can gradually transition from rectangular to the circular to provide a smooth transition. The composition of the inner core can be varied along the length of the braid.

Abstract: Implants or sensors often include and rely on inductive and ferromagnetic electrical components to measure and communicate data outside of the body to an external device, creating a safety concern when a patient with these implants or sensors must undergo an MRI scan. Further, various external devices that include inductive and ferromagnetic electrical components are exposed to potentially damaging MRI scans. An electrical coil assembly can include an electrical coil that includes a substrate and an electrical conductor supported by a first face of the substrate. In an example, the electrical coil assembly further includes a fuse element that is configured to move from a disengaged position in which the electrical fuse conductor is out of contact with the electrical conductor to an engaged position in which the electrical fuse conductor contacts the electrical conductor so as to define a short circuit.

Abstract: Various exemplary methods and devices are provided for fixing bone anchors to bone. In general, the methods and devices can allow for a bone anchor to be fixed to a bone at a desired angle to a receiver member. In an exemplary embodiment, a bone anchor assembly is provided that includes a bone anchor configured to engage bone, a receiver member that seats a spherical head of the bone anchor and a spinal fixation element, a compression member seated within the receiver member, proximally of the head of the bone anchor, and a closure mechanism seated within the receiver member, proximally of the compression member. One or more of the receiver member, the compression member, and the closure mechanism can have gripping features thereon configured to secure the bone anchor and/or the spinal fixation element within the receiver member, thereby reducing a risk of slippage of the bone anchor and/or the spinal fixation element with respect to the receiver member.

Abstract: A delivery member is provided for delivering and deploying an intravascular medical device. The delivery member includes a flexible distal portion including a wound wire coil surrounded by a flexible sleeve and inhibited from extending lengthwise by a stretch resistant member positioned through the lumen of the coil. The delivery member can include hypotubes positioned on either side (distally and proximally) from the wound wire coil to which the stretch resistant member and the wound wire coil can be attached.

Abstract: An assembly at a proximal end of an intravascular delivery system can allow the proximal end of a pull wire to move independently of a delivery tube. The assembly can generally include the pull wire, the delivery tube, a feature to prevent the proximal end of the pull wire from becoming inaccessible due to distal movement of the pull wire, and a feature to protect the proximal end of the pull wire from inadvertent, premature manipulation. When the intravascular delivery system is navigating tortuous vasculature, the proximal end of the pull wire can move distally in relation to the proximal end of delivery tube, relieving stress on the distal end of the pull wire. The proximal end of the pull wire can be protected from inadvertent manipulation during delivery and made available for manipulation once the distal end of the delivery system is in place.

Abstract: An orthopaedic surgical instrument includes a customized patient-specific surgical instrument having a body. The body has a bone-facing surface and an outer surface positioned opposite the bone-facing surface. The body includes a number of bone-contacting segments raised relative to the bone-facing surface. The bone-contacting segment include negative contours shaped to match corresponding positive contours of a patient's bone. The positive contours correspond to silhouette curves of a three-dimensional model of the patient's bone that correspond to contours of the patient's bone captured in images used to generate the model. The body further includes a number of surgical guides extending from the outer surface to the bone-contacting surface or the bone-facing surfaces. A method associated with the instrument is also disclosed.

Abstract: Systems and apparatus for reliably sealing a surgical device are disclosed herein. Specifically, a surgical device including a drive shaft tube that is coupled to a drive shaft is disclosed. Because the drive shaft tube is coupled to the drive shaft, the drive shaft tube rotates at the same rotational speed as the drive shaft, which is less than the rotational speed of a cannulated motor shaft. The drive shaft tube can extend through the cannulated motor shaft. In addition, a sealing member can be provided to seal between the drive shaft tube (which rotates slowly) and the motor instead of between the motor shaft (which rotates more quickly) and the motor. The sealing member can be provided in a gap defined between an outer surface of a portion of the drive shaft tube extending beyond the cannulated motor shaft and the motor.

Abstract: A bone implant kit includes an implant and first and second electrical stimulation anchors. The implant defines an inner surface inner configured to face a bone to which the bone implant kit is configured to attach, and an outer surface opposite the inner surface. The implant further defines first and second bone fixation holes that each extend from the inner surface to the outer surface. The first and second bone fixation holes are spaced from each other along a longitudinal direction. The first electrical stimulation anchor can be sized and configured for insertion into the first bone fixation hole, and the second electrical stimulation anchor can be sized and configured for insertion into the second bone fixation hole. The first and second electrical stimulation anchors can be configured to respond to a magnetic field so as to generate an electric field between the first and second electrical stimulated anchors.

Abstract: A method of preparing a shoulder to receive a glenoid component includes accessing a glenoid of a shoulder, positioning a distal portion and a proximal portion of a combination power extension/anti-rotation device on a guide wire positioned in the shoulder and reaming a hole in the shoulder using the combination power extension/anti-rotation device with the distal portion and the proximal portion positioned on the guide wire. The proximal portion is removed from the guide wire and pivoted with respect to the distal portion while the distal portion is still positioned on the guide wire. The picoted proximal portion is used to rotate an instrument to a first position and a bore is formed in the glenoid through the instrument with the instrument at the first position.

Abstract: A surgical procedure method includes accessing an implanted joint prosthesis having an implant engaged within a bone of the joint and a first articulating component mounted by a first mating component to a first insert component removably mounted to the implant, and partially disassembling the accessed implanted joint prosthesis by removing the first insert component with the first articulating component fixed thereto from the implant while the implant is engaged with the bone. The angular position of the first mating component with respect to the first insert component is then determined and replicated with a second insert component and a second mating component. The second insert component and the second mating component are then fixed at the replicated angle and the fixed second insert component and second mating component are mounted to the implant engaged within the bone. A new articulating component is then mounted to the second mating component.

Abstract: An example system can include a tubular braid, a catheter, and an embolic coil. The tubular braid can have an open end, a pinched end, and a predetermined shape. In the predetermined shape, the tubular braid can have two inversions and a middle segment extending between the two inversions that forms a sack. The tubular braid can be implanted in an implanted shape based on the predetermined shape. A distal end of the catheter can be inserted into the sack when the tubular braid is implanted. The embolic coil can be delivered through the catheter into the sack. The opening to the sack can correspond to a constricted columnar segment of the middle segment when the braid is in the predetermined shape.

Abstract: The disclosure relates to an endoscopic light source that includes a first emitter. The first emitter may emit light of a first wavelength at a dichroic mirror which reflects the light of the first wavelength to a plurality of optical fibers. The endoscopic light source further comprises a second emitter. The second emitter may emit light of a second wavelength at a second dichroic mirror which reflects the light of the second wavelength to the plurality of optical fibers. In one embodiment, the first dichroic mirror may be transparent to the light of the second wavelength, allowing the light of the second wavelength to pass through the first dichroic mirror.

Abstract: A bone plate system for internal fixation of bone fractures includes a bone plate having a plurality of bone plate holes. The holes are constructed to receive either a non-locking, locking, or variable-angle locking bone screw. The holes have discrete columns of teeth or thread segments arranged around the inner surface of the hole for engaging threads on the heads of locking and variable-angle locking bone screws. Conventional locking bone screws engage the bone plate coaxially with the central axis of the bone plate hole. Variable-angle locking bone screws can engage the bone plate at a selectable angle within a range of selectable angles relative to the central axis of the bone plate hole. The head of the variable-angle locking screw is at least partially spherical, and the thread thereon has a profile that follows the arc-shaped radius of curvature of the spherical portion of the screwhead.

Abstract: Systems and methods are disclosed herein that can allow for wirelessly powering and/or communicating with a sterile-packed electronic device without removing the electronic device from its sterile packaging and while maintaining the sterility of the electronic device. In some embodiments, a base station with a power transmitter wirelessly transfers power to a power receiver of the electronic device, for example using inductive, capacitive, or ultrasonic coupling. The base station or another external device can also be used to wirelessly program or interrogate the electronic device. Battery charging circuits and switching circuits for use with said systems and methods are also disclosed.

Abstract: A method of treating an aneurysm, including determining a diameter associated with a vessel having the aneurysm; selecting one of a plurality of braided implants for treating the vessel, wherein each braided implant comprises a porosity substantially consistent over up to a 1 mm diameter range, each braided implant configured to provide consistent porosity over different diameter ranges; and treating the vessel with the one of the plurality of braided implants.