Abstract: A system effectively narrows a patulous Eustachian tube (ET) of a patient with a guide catheter, instrument, and insert. The guide catheter includes a shaft, a lumen and a distal end configured to provide access the ET when the guide catheter is inserted into a head of the patient. The instrument comprises a shaft. The insert comprises a body configured to radially expand and retract between a non-expanded state and an expanded state. The insert is sized and shaped to be received within the first lumen when in the non-expanded state and is operable to expand to the expanded state to substantially reduce an effective diameter of the ET.

Abstract: An implanted device, such as an inferior vena cava filter, that is partially embedded in soft tissue is retrieved by coupling a vibration device to the implanted device. The implanted device is disembedded from the soft tissue at least in part by generating a vibration with a vibration generator, transmitting the vibration along the vibration transmission apparatus to the implanted device, and vibrating the implanted device. The implanted device is then moved away from the embedding site. A medical device assembly includes the vibration generator, the implantable device and the vibration transmission apparatus.

Abstract: An atherectomy device comprising a rotatably motor-driven flexible hollow shaft that is coaxial with a longitudinal axis of the guidewire; an annular distal end of the hollow shaft having a diameter that is only slightly larger than the diameter of the guidewire and configured with cutting surfaces for piercing hardened atherosclerotic plaque! a tubular sleeve secured to a first peripheral surface of the hollow shaft and configured with cutting surfaces for enlarging an opening formed in the plaque; and an asymmetric cutting unit extending between the sleeve and a second peripheral surface of the hollow shaft, to enable eccentric rotation of the hollow shaft for cutting and removing additional occlusive material from the blood vessel to open a chronic total occlusion. In one embodiment, the cutting unit is a helical strand unit having a polygonal cross section with a first side that atraumatically contacts a blood vessel wall.

Abstract: A tool for a medical instrument includes a stationary component, a branch which is pivotable relative to the stationary component about a pivot axis, a transmission device for transmitting a force to the pivotable branch, and a coupling device for coupling the transmission device to the pivotable branch in such a way that a translation of the transmission device entails a pivoting movement of the pivotable branch about its pivot axis. The coupling device includes several coupling portions on the pivotable branch and several coupling portions on the transmission device. Each coupling portion on the pivotable branch is assigned to a corresponding coupling portion on the transmission device. The coupling portions are arranged and designed such that the coupling of pivotable branch and transmission device is effected, depending on the positions of pivotable branch and transmission device, by different pairs of corresponding coupling portions.

Abstract: A calculus removing device includes a retaining portion (e.g., a wire or gel), a cylinder, an introduction tube, and a hand-operated unit. The retaining portion is configured to retain calculi and broken calculus pieces. The cylinder includes a storage portion configured to store the calculi, an opening communicating with the storage portion, and an introducing portion configured to permit the retaining portion to be introduced into the storage portion. The introduction tube is provided with a lumen which allows introduction of the retaining portion into the storage portion via the introducing portion. The hand operating unit is provided with an operating member configured to operate the introduction of the retaining portion into the storage portion.

Abstract: A clip having a delivery shape and an implanted shape has a first and a second leg joined at their distal ends at a distal point of the clip. The distal point forms a tapered shape of the clip and is adapted to pierce tissue. Proximal ends of the first and second legs are spaced apart in the delivery shape by a first distance. The proximal ends are compressible to the implanted shape in which the legs are spaced apart by a second distance that is shorter than the first distance. A related delivery device, a related system, and a delivery method are also disclosed.

Abstract: A surgical instrument system that includes a housing and a rotatable drive shaft, a motor operably coupled to the drive shaft, and a plurality of replaceable end effectors that can be connected to the housing. Each replaceable end effector includes a drive screw that is turned a fixed number of revolutions by the motor-driven rotatable drive shaft when the end effector is connected to the housing. Each end effector further comprises a firing member operably coupled with the drive screw of the end effector. The drive screw is configured to displace the firing member over a firing length as a result of the fixed number of revolutions. In certain embodiments, each replaceable end effector can include a drive screw with a thread pitch set to the firing length divided by the fixed number of revolutions.

Abstract: A device that helps clear a fluid or other material lodged in a person's throat has a barrel with an open proximal end and an opening laden distal end. A plunger is slidably disposed within the barrel such that the plunger, by being manually drawn outwardly, creates suction within the barrel drawing air through the opening. A single or multi-section tube, flexible on at least its distal end, is fluid flow connected to the opening and has a face mask along its length. The distal end of the tube is intubated with a person proximate the fluid or other material so that as the plunger is drawn outwardly through the barrel, the suction created within the barrel causes air to be drawing in through the tube and into the barrel thereby helping draw out and dislodge the fluid or other material. A backflow valve located on the barrel helps clear the barrel of such things as vomit that might have been drawn into the barrel.

Abstract: Implementations of the present disclosure relate to apparatuses, systems, and methods for anastomosing vascular systems in medical procedures. A pair of similar or identical coupling devices may be disposed at the ends of two vessels, either natural or synthetic. The coupling devices may be capable of hermaphroditically connecting to one another to provide a simple and secure connection which promotes growth of the vessels between the bio-absorbable coupling devices.

Abstract: A blade assembly comprising: a tip including two or more tubes, wherein the two or more tubes include at least: an outer tube and an inner tube; and a mechanical enclosure including: a locking spline having a longitudinal axis; and a slide lock; wherein the slide lock slides along the longitudinal axis of the locking spline and over the locking spline forming a locked state so that rotational movement of the locking spline, around the longitudinal axis of the locking spline, is prevented; and wherein the outer tube is coupled to the locking spline so that rotational movement of the outer tube, around the longitudinal axis of the locking spline, is prevented during the locked state.

Abstract: A stent delivery assembly includes a delivery balloon defining a balloon axis, and a stent disposed around the delivery balloon. The stent has interconnected struts, and the delivery balloon has a balloon surface with a number of strips that are disposed on the balloon surface and extend along the balloon axis, the strips having an unhydrated state and a hydrated state, the strips having a smaller volume in the unhydrated state than in the hydrated state. For a stent composed of axially aligned segments connected via connectors disposed between adjacent ones of the segments, the strips have a length greater than an axial distance between axially outermost connectors connecting the adjacent ones of the segments.

Abstract: The present disclosure describes systems and methods for pressure-driven micro-surgical tool actuation. The systems and methods may encompass the use of a remote handle held by a first hand of a user as well as a surgical tool located in the eye of a patient. A primary actuator may be included in remote handle and operable to be actuated by a mechanical force exerted on the handle. Actuating the primary actuator pressurizes a fluid within a length of tubing. The pressurized fluid may be transmitted to a dynamic tool held by a second hand of the user, where the pressurized fluid may be used to actuate a subordinate actuator. Actuation of the subordinate actuator may actuate a dynamic component of the dynamic tool.

Abstract: A vein harvesting device is disclosed. The vein harvesting device includes a handle assembly, at least one elongated portion, first and second end effectors, and a tip. Each end effector is disposed adjacent a distal portion of the at least one elongated portion. Each end effector includes a first jaw member and a second jaw member, and at least one jaw member is movable toward the other jaw member. The tip is disposed in mechanical cooperation with the elongated portion. A distal end of the tip extends distally beyond a distal-most end of the first end effector. The first end effector is movable independently of the tip, and the second end effector is movable independently of the tip.

Abstract: Systems, devices and methods for managing surgical instruments throughout their lifecycle include disabling a usage based device lockout and providing notifications for devices nearing a usage based lockout. A device adaptor connected inline between a surgical instrument and a power source can be configured to alter a device EEPROM to allow for additional device usage despite a usage based lockout. Notifications and user prompts may be displayed requiring a user to acknowledge that a usage based device lockout has occurred in order to avoid an attempt to use an expired device in a future procedure.

Abstract: A system for controlling displacement of an intervention device having an end for inserting in a patient body, including a base in a fixed position relative to the patient. A first portion has an arc member and is pivotally mounted on the base around a first axis (A1). A second portion includes a support member and a carrier member. The support member partially rotates around a second axis (A2). A third portion includes a holding member, and a sliding member mounted on the support member along a translation axis (AT). The holding member is arranged so that translation of the sliding member causes the intervention device to translate along a third axis (A3). The third axis (A3) is parallel to and offset from the translation axis (AT). When the carrier member is positioned halfway of the arc member, the first (A1), second (A2) and third (A3) axes are orthogonal.

Abstract: A device for robot-assisted surgery, comprising at least one non-sterile manipulator arm (12) having a coupling unit (100) with drive elements. The device further has an instrument unit (300) which comprises a surgical instrument (500) and a sterile sterile unit (400) for coupling the surgical instrument (500) to the drive elements of the coupling unit (100). The coupling unit (100) comprises a translatory drive element (110, 112) for generating a translatory drive movement and a rotatory drive element (114, 116) for generating a rotatory drive movement. The sterile unit (400) has a translationally driven element (408, 410) couplable to the translatory drive element (110, 112) and a rotationally driven element (412, 414) couplable to the rotatory drive element (114, 116). The device has a sterile lock (200) which is capable of being coupled to the coupling unit (100) and to the sterile unit (400).

Abstract: A trocar wound closure system includes a suture passing needle and a guide for directing the needle through the wound site. A distal portion of the needle includes a capture rod with a slot. An obturator tube with a cutout section can be axially actuated to align the cutout section with the slot, and then moved out of alignment so as to capture the suture. The guide includes at least two tracks for directing the needle through the tissue track. A suture catcher is located adjacent to the exit of each track, and configured to be actuated from a radially extended configuration to a retracted configuration so as to capture the suture section inserted through each loop. Radially expandable arms at distal section are movable between an expanded configuration and a slender configuration.

Abstract: A modular valve prosthesis includes an inflow stent, a valve component including a valve stent and a prosthetic valve, and an outflow stent. In a radially compressed delivery configuration, an inflow end of the valve stent is separated from an outflow end of the inflow stent and an outflow end of the valve stent is separated from an inflow end of the outflow stent. In a radially expanded deployed configuration, the inflow end of the valve stent is in contact with the outflow end of the inflow stent and the outflow end of the valve stent is in contact with the inflow end of the outflow stent. A delivery system includes a capsule including first, second and third sections and flexible first and second bands between respective sections. The modules of the modular valve prosthesis are aligned with the sections and gaps between the modules are aligned with the bands.

Abstract: Stent delivery systems and methods for making and using stent delivery systems are disclosed. An example stent delivery system may include an inner shaft. A deployment sheath may be disposed about the inner shaft. A stent may be disposed between the inner shaft and the deployment sheath. A stent reconstraining member may be secured to an inner surface of the deployment sheath and releasably secured to the stent.

Abstract: A vein harvesting device is disclosed. The vein harvesting device includes a handle assembly, an elongated portion extending distally from the handle assembly and defining a longitudinal axis, an end effector, and a retractor. The end effector is disposed adjacent a distal portion of the elongated portion, and includes a first jaw member and a second jaw member. At least one jaw member is movable toward the other jaw member. The retractor is disposed in mechanical cooperation with the elongated portion, and includes a shaft and a pair of legs. The retractor is movable from a non-deployed position where the shaft is aligned with the longitudinal axis, to a deployed position where the shaft is disposed at an angle with respect to the longitudinal axis.