Abstract: Endoscopic light refraction imaging techniques are described for configuring a viewing trocar and/or angled endoscope with a light refracting element, such as glass and/or plastic prism for instance. The light refracting element can be utilized in and/or with the viewing trocar to refract (i.e., bend) light passing into the trocar through the trocar's window. As a result, the angled endoscope's field of view can be substantially aligned with the field of view of the trocar's window, thus allowing the angled endoscope and viewing trocar to be used together to create ports in a patient, including initial ports of endoscopic surgical procedures.

Abstract: An aneurysm treatment system can include an embolic implant, a delivery system, and a handle member that are collectively designed so that the combination of the handle member and the delivery system can be used as a deployment apparatus for the embolic implant. A proximal extension of the delivery tube can be placed inside a handle channel of handle member and the handle member can be manipulated to cause the proximal extension to bend to a predetermined angle with respect to the delivery tube, thereby separating the proximal extension from the delivery tube at a disconnection feature between the proximal extension and the delivery tube. The delivery tube includes a lumen having a pull wire that runs through the delivery tube and into the proximal extension. The proximal extension, pull wire, and handle member can be translated proximally in relation to the delivery tube to deploy the embolic implant.

Abstract: An implant including an open end and a pinched end can have a predetermined shape. When in the predetermined shape, the tubular braid can include a proximal inversion and two segments, and the braid can be composed of one or more wires. The first segment can extend from the open end of the tubular braid to the proximal inversion. The second segment can be at least partially surrounded by the open end and extend from the proximal inversion to the pinched end. The tubular braid can also include at least one corrugated fold. The one or more corrugated folds can be located within the first segment, second segment, or both. The corrugated folds can be configured to assist in anchoring the example device when in the implanted shape within an aneurysm in a similar manner to stent struts to help the tubular braid hold its shape.

Abstract: A method for constructing a braided implant delivery system and treating an aneurysm can include attaching a braided implant having a band attached thereto to a delivery tube, positioning the braided implant within the aneurysm, and releasing the band from the delivery tube, thereby releasing the braided implant. The band can include movable extensions that can press into an outer surface of the delivery tube to secure the band to the delivery tube then move away from the outer surface of the delivery tube to release the band. A pull wire can be engaged to the band to secure the band to the delivery tube then be pulled proximally to release the band from the delivery tube. At least a portion of the braid of the braided implant can be positioned within a lumen of the delivery tube.

Abstract: Female polyaxial joints for connecting a strut to a support frame of an external fixation device are described having a ball socket and a ball member. The ball member includes a spherical portion and a ball member shaft extending from the spherical portion. At least one aperture is positioned on the ball member and traverses through at least a portion of the ball member shaft. An internal surface of the ball member shaft may be threaded and configured to receive a threaded connector.

Abstract: An orthopaedic surgical instrument system for use during a surgical procedure to implant an orthopaedic knee prosthesis includes a tibial trial component adapted to be positioned on a surgically-prepared proximal end of a patient's tibia. The tibial trial component has a base plate and a central post extending upwardly from a superior surface of the base plate. A superior surface of the central post has a ramp surface defined therein, with the ramp surface inclining superiorly in the anterior-to-posterior direction.

Abstract: Stents generally can include a tubular structure having circumferentially positioned undulating wires that extend over a majority of a length of the stent such that the undulations oscillate circumferentially to define a circumference of the stent. The undulations can wrap over and under adjacent undulations to form an interwoven structure. Additionally, or alternatively, adjacent wires can be joined. Wires forming the stent can be cut from elastic tubing such that each wire has a three-dimensional shape.

Abstract: Instrumentation and methods are provided for orthopedic surgery, including bone distraction. The application describes a bone distraction system that can be used to both distract and retract, or increase and decrease, a gap between first and second bone segments. The instrumentation can include any one of, or any combination of, a distractor, a ratchet, a first footplate, a second footplate, a first torque application instrument, and a second torque application instrument.

Abstract: Embodiments of a hybrid imaging sensor that optimizes a pixel array area on a substrate using a stacking scheme for placement of related circuitry with minimal vertical interconnects between stacked substrates and associated features are disclosed. Embodiments of maximized pixel array size/die size (area optimization) are disclosed, and an optimized imaging sensor providing improved image quality, improved functionality, and improved form factors for specific applications common to the industry of digital imaging are also disclosed.

Abstract: Embodiments described include devices and methods for forming a porous polymer material. Devices disclosed and formed using the methods described a spacer for spinal fusion, craniomaxillofacial (CMF) structures, and other structures for tissue implants.

Abstract: The present disclosure is directed to a method of surgical repair utilizing a continuous compression staple for an orthopedic injury site having a long bone fracture defining a fracture boundary between a first bone fragment and a second bone fragment. The method can include the steps of aligning the fragments, applying a temporary compressive force to the aligned fragments, inserting a compression staple in a tensioned state into the first and second bone fragments such that it traverses the fracture boundary, releasing tension in the compression staple such that the staple exerts a continuous compressive force to the first and second bone fragments, and securing a neutralization implant to the long bone. The disclosure further includes kits and systems for performing the disclosed surgical methods.

Abstract: A radially compressive implant, which includes a central vertical axis, is configured to transition between a natural shape and an insertion shape. A transition of the implant from the natural shape to the insertion shape facilitates the implant storing energy deliverable radially relative to the central vertical axis. A transition of the implant from the insertion shape toward the natural shape facilitates the implant delivering the energy stored therein radially relative to the central vertical axis. An implant delivery device in an implant engagement position is configured to engage the implant and constrain the implant in the insertion shape. The implant delivery device in an implant release position is configured to release the implant.

Abstract: A detachment system configured to deliver an implantable medical device to a target location of a body vessel includes a generally hollow distal tube and an engagement system. The distal tube can have an inner lumen having a first diameter therethrough and a narrowed portion positioned on at least a portion of the distal tube and having a second diameter lesser than the first diameter. The engagement system can be slidably disposed within the inner lumen and have a detachment feature connected to the implantable medical device and a locking member engaging the detachment feature and interfacing with the narrowed portion of the distal tube. The locking member is configured to deploy the implantable medical device when the locking member is displaced from the narrowed portion of the distal tube.

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: An orthopaedic system and method to assemble an orthopaedic prosthesis is disclosed. The system may also include prosthetic trial components, which may be used to size and select the components of the orthopaedic prosthesis. The system may include components of the orthopaedic prosthesis such as, for example, a prosthetic femoral component, a prosthetic tibial component, a prosthetic stem component, and a prosthetic sleeve component.

Abstract: The present invention provides a braided implant with a retractable dual proximal layer and methods for administering the braided implant to treat aneurysms. The implant can include a tubular braid that can be set into a predetermined shape, compressed for delivery through a microcatheter, and implanted in at least one implanted position that is based on the predetermined shape and the geometry of the aneurysm in which the braid is implanted. The implant can also have a retractable ball segment at the proximal end of the device made of the same braid that can be heat treated into an ellipsoid shape. The retractable ball segment can be movable from a position outside the aneurysm to a position at least partially enclosed within the implant to increase or decrease the height of the implant relative to the aneurysm or better conform the implant to the neck of the aneurysm.

Abstract: A system for providing illumination for an endoscope device. The system includes a light source comprising light bundles, wherein each light bundle comprises light emitters. The light source sequentially pulses electromagnetic energy in individual electromagnetic partitions, where each of the plurality of light bundles corresponds to one of the individual electromagnetic partitions. The system includes an electromagnetic sensor embedded within the light source to sense electromagnetic energy emitted from at least one, but less than all, of the light emitters within each of the light bundles. The system includes a control circuit in electronic communication with the electromagnetic sensor and at least one of the light emitters, wherein the electromagnetic sensor receives electromagnetic energy from at least one of the light emitters, and wherein the electromagnetic sensor measures an amount of electromagnetic energy generated by the at least one of the light emitters.

Abstract: Various exemplary methods and devices are provided for passing sutures around anatomical structures. In an exemplary embodiment, a suture delivery device is provided that includes a body portion having a suture delivery member disposed therein and configured to pass a suture around an anatomical structure. The suture delivery member can be movable between a retracted configuration in which the suture delivery member is disposed within the body portion and an advanced configuration in which the suture delivery member extends distally beyond the body portion and assumes an arcuate shape. The arcuate shape can correspond to a shape of the anatomical structure and can extend almost all of the way around the anatomical structure, for example at least around 270° of a circle, thus assisting a user in passing the suture around the anatomical structure without having to manually manipulate the suture delivery device at awkward angles around adjacent tissue.

Abstract: A braid for treating an aneurysm can include a first radially expandable segment operable to move from a collapsed state within a microcatheter to a deployed state distal of the microcatheter. The first radially expandable segment can be capable of radially expanding to form an outer occlusive sack in the aneurysm in the deployed state. The braid can also include a second radially expandable segment operable to move from the collapsed state within the microcatheter to the deployed state distal of the microcatheter, wherein the second radially expandable segment is capable of radially expanding inside the outer occlusive sack to form an inner occlusive sack in the outer occlusive sack in the deployed state. An expansion mechanism can be included and be disposed at a proximal end of the first and second radially expandable segments.