Abstract: A soft anchor assembly according to an exemplary aspect of the present disclosure includes, among other things, a sheath and a flexible strand at least partially surrounded by the sheath.

Abstract: A left atrial appendage (LAA) closure device that includes an anchor portion having a first segment and a second segment that are connected in spaced-apart manner by a first connector, a sealing portion, and a second connector that connects the anchor portion and the second segment sealing portion. The first segment is adapted to be positioned outside the LAA and in the pericardial sac after deployment of the closure device, and the second segment is positioned between the first segment and the sealing portion inside the LAA.

Abstract: The present invention provides a catheter for treating an occlusion in a body lumen. The catheter includes an elongated tube, a first electrode pair and a second electrode pair each configured to generate shock waves. The catheter also includes a flexible polymer enclosure that is fillable with conductive fluid and wrapped circumferentially around at least a portion of the elongated tube such that it surrounds the first and second electrode pairs. The first and second electrode pairs can be arranged relative to one another to promote interference between shock waves generated at the electrode pairs when voltage is delivered across the electrodes of each pair. Electrode pairs can be longitudinally adjacent (spaced a relatively small longitudinal distance apart), longitudinally aligned (at the same longitudinal location), circumferentially offset (offset about the circumference of the catheter), circumferentially aligned (at the same circumferential location), or any combination of any of the above.

Abstract: Methods for surgical navigation use a trajectory frame/guide assembly for use with surgical navigation systems that includes a base having a patient access aperture formed therein. A yoke is mounted to the base and is rotatable about a roll axis. A platform is mounted to the yoke and is rotatable about a pitch axis and interchangeably holds a single lumen or multi-lumen guide array and a device guide. A device guide can be rotated to align an access channel with a desired lumen path. No x-y actuators are required and a virtual guide array may also or alternatively be used to identify a desired open channel in the device guide for the preferred trajectory path.

Abstract: An ultrasonic osteotome bit, comprising a bit bar (1), a bit body (3), and a bit grinding portion (2) located at a front end of the ultrasonic osteotome bit. The bit grinding portion (2) is in the shape of a triangular pyramid, the bottom face of the triangular pyramid is the rear end of the bit grinding portion (2), and the tip of the triangular pyramid directly facing the bottom face is the front end of the bit grinding portion (2). One end of the bit bar (1) is connected to the rear end of the bit grinding portion (2), and the other end of the bit bar (1) is connected to the bit body (3). Two of the three lateral pyramidal faces of the triangular pyramid are respectively used as a first grinding face (21A) and a second grinding face (21B). By means of the ultrasonic osteotome bit, a normal bone-grinding operation can be completed, and since the front end thereof is small in area, the grinding speed is high.

Abstract: In one embodiment, the present disclosure relates to a probe for use in minimally invasive surgery. The probe includes a shaft and a tip extending from the shaft. The tip includes a bulbous shape with a smooth and rounded outer surface. In some embodiments, the shaft is separated from the tip by a neck such that both the shaft and the tip expand outward from a concave surface of the neck. In some embodiments, one or both of a neuromonitoring element and an ultrasound sensor are disposed on the tip. In some embodiments, a probe may include a surface feature that resists expulsion of the probe from a human body when the probe is disposed in the human body. In further embodiments, a probe may include insulated material over a first surface region and conductive material over a second surface region.

Abstract: An endoluminal needle or punch is describes wherein the distal end of the endoluminal needle is able to articulate laterally out of the longitudinal axis of the steerable endoluminal needle. The endoluminal needle further comprise a blunted distal end configuration that is minimally traumatic. Under control by the user, at the proximal end of the endoluminal needle, a sharp stylet can be advanced to punch tissue and then be retracted to maximize safety. The endoluminal needle is configured for use within an introducer.

Abstract: An embodiment of the invention includes an expandable implant to endovascularly embolize an anatomical void or malformation, such as an aneurysm. An embodiment is comprised of a chain or linked sequence of expandable polymer foam elements. Another embodiment includes an elongated length of expandable polymer foam coupled to a backbone. Another embodiment includes a system for endovascular delivery of an expandable implant (e.g., shape memory polymer) to embolize an aneurysm. The system may include a microcatheter, a lumen-reducing collar coupled to the distal tip of the microcatheter, a flexible pushing element detachably coupled to an expandable implant, and a flexible tubular sheath inside of which the compressed implant and pushing element are pre-loaded. Other embodiments are described herein.

Abstract: Delivery devices for delivering an ophthalmic device into an eye. In some embodiments the delivery devices are adapted to deliver an intraocular lens into an eye.

Abstract: A tissue removal device including customizable tips and method of use thereof. The tissue removal device may include an outer shaft having a removable tip attached to the outer shaft and a rotatable inner shaft extending through the outer shaft and having a rotatable cutting portion extending from the inner shaft. Disc material may be cut and removed from a surgical area using an auger-like and/or suction mechanism to facilitate the transfer of removed tissue away from the surgical area.

Abstract: An obstruction removal device is described, having one or more engaging members which can engage portions of the clot. The one or more engaging members have a collapsed, delivery state, and an expanded, deployed state.

Abstract: A method of performing a surgical procedure with a surgical tool assembly includes inserting a surgical tool into a passage of a patient. The surgical tool can include a main unit and a first rigid sheath. The main unit includes an inner tube that is received within an outer tube. The first rigid sheath removably receives the main unit. The surgical tool can be removed from the passage of the patient, and the first rigid sheath can be completely removed from the main unit. A second rigid sheath having a different shape from the shape of the first rigid sheath can then be removably attached to the main unit instead of the first rigid sheath.

Abstract: A surgical instrument includes an articulation assembly having a dual threaded rod, a first nut, a second nut, a first articulation rod, and a second articulation rod. The dual threaded rod includes a body, a first thread encircling at least a portion of the body in a first direction, and a second thread encircling at least a portion of the body in a second, opposite direction. Rotation of the dual threaded rod in a first direction relative to the elongated portion causes the first nut to move distally relative to the dual threaded rod. Rotation of the dual threaded rod in the first direction relative to the elongated portion causes the second nut to move proximally relative to the dual threaded rod. The first articulation rod is coupled to the first nut and the end effector, and the second articulation rod is coupled to the second nut and the end effector.

Abstract: An implant unit delivery tool is provided. The implant delivery tool may include a body, a holder disposed at a distal end of the body and adapted to hold an implant unit, and an implant activator associated with the body, the implant activator configured to receive power from a power source. The implant activator may be configured to selectively and wirelessly transfer power from the power source to the implant unit during implantation of the implant unit into the body of a subject to cause modulation of at least one nerve in the body of the subject, and determine a degree of nerve modulation response resulting from the selective and wireless transfer of power from the power source to the implant unit claims.

Abstract: Devices, methods and systems are described that enable achieving a working diameter that is greater than a resting diameter and to stimulate fluid circulation during high-speed rotation. The drag coefficient of the drive shaft is increased and, in some embodiments, the mass is increased. Among other advantages, the resulting drive shaft with an eccentric element integrated with and/or attached thereto will achieve orbital motion at a rotational speed that is less the rotational speed required to achieve orbital motion without the increased drag coefficient. The concomitant increase in fluid flow and/or fluid stirring at a comparatively lower rotational speed is a further advantage. These characteristics may allow, therefore, a smaller diameter abrasive element to be used which is advantageous in small and/or highly tortuous vessels.

Abstract: Various example embodiments described herein are directed to articulating surgical instruments for treating tissue comprising an end effector and a shaft extending proximally from the end effector along a longitudinal axis. In certain embodiments, the shaft comprises a plurality of transverse spacer members as well as first and second rotatable members extending through at least a portion of the plurality of transverse spacer members. The first and second rotatable members may both be biased away from the longitudinal axis such that their respective directions of bias vary with rotation of the first rotatable member. When the respective directions of bias of the first and second rotatable members oppose one another, the shaft may be substantially straight. When the respective directions of bias of the first and second rotatable members are aligned with one another, the shaft may articulate away from the longitudinal axis in the direction of the alignment.

Abstract: An end effector assembly of a surgical system includes a blade and a jaw member movable relative to the blade between a spaced-apart position and an approximated position for clamping tissue. The blade defines a first width and the jaw member defines a second width wider than the first width. The jaw member defines a first side facing the blade and a second side facing away from the blade. A marking is formed on the second side of the jaw member facing away from the blade. The marking defines a third width substantially equal to the first width of the blade to allow a surgeon to visualize a width of the blade when the blade is not visible.

Abstract: Particular embodiments disclosed herein provide a rotational cutter for delaminating a membrane from a retina of an eye. The rotational cutter may comprise a first shaft and a second shaft comprising a blade portion, wherein the second shaft is coupled to a driver that is configured to at least partially rotate the second shaft relative to the first shaft, wherein rotating the second shaft rotates the blade portion for delaminating the membrane. The rotational cutter may also comprise a bottom portion configured to interface with a surface of the retina, wherein the bottom portion comprises one or more curved edges.

Abstract: The present invention relates to a puncture device for creating a TIPS shunt, comprising a puncture needle, a sheath, the sheath being arranged to surround the puncture needle, the puncture needle being slidably arranged inside the sheath so that the puncture needle can be moved between a first position in which the puncture needle protrudes beyond the distal end of the sheath and a second position where a tip of the puncture needle is retracted into the sheath, the sheath and the puncture needle being arranged so that in the second position, blood can be aspirated into the sheath through a gap between the puncture needle and the sheath, a locking means, the locking means being arranged for releasably locking the puncture needle in the first and/or the second position.

Abstract: Devices and methods used to drain a spinal cyst are disclosed. An opening may be created by a medical device, such as a nested needle assembly, that is inserted percutaneously into a facet joint adjacent to the cyst. The needle assembly may include a first elongate member, needle or introducer cannula; a second elongate member, inner cannula, needle, or trocar; and a piercing needle. The piercing needle may be used to microfenestrate a wall of the cyst such that fluid within the cyst is permitted to drain from the cyst.