Abstract: Embodiments of a surgical instrument and its methods of use are disclosed. The disclosed embodiments of a surgical instrument may include a handle and an elongated shaft assembly distally extending from the handle. The elongated shaft assembly may include an articulable portion. An articulation control may be associated with the elongated shaft assembly. The articulation control may be movable between a first position in which the elongated shaft assembly is arranged in a first articulation position and a second position in which the elongated shaft assembly is arranged in a second articulation position. The surgical instrument may include a fastener deployment system with a locking member. The articulation control may block movement of the locking member when the articulation control is located in the first position. The articulation control may also permit movement of the locking member when the articulation control is located in the second position.

Abstract: A surgical fastener and a related deployment device as well as their methods of use are disclosed. In one embodiment, the deployment device includes one or more surgical fasteners including a head and a distally extending coil body attached to the head. The head includes a through hole with an internal thread. The deployment device also includes a mandrel including a threaded portion located at a distal end of the mandrel. The threaded portion is engaged with the internal thread of the one or more surgical fasteners. A rotator is associated with the one or more surgical fasteners such that the rotator can selectively rotate the one or more surgical fasteners relative to the mandrel to displace the one or more surgical fasteners in a distal direction.

Abstract: A deployment device for positioning a soft tissue repair prosthesis includes a self-expanding support body releasably attachable to the prosthesis. The support body may be removably insertable into a pocket of the prosthesis. A handle coupled to the support body facilitates positioning the patch and/or removal of the support body from the pocket. The support body may substantially occupy the pocket in an expanded configuration. The handle may be arranged to direct a pulling force to the outer peripheral edge of the support body and/or cause a portion thereof to be pulled downward and below the body during withdrawal of the deployment device from the prosthesis. The support body may include support segments pivotally coupled together and foldable to collapse the support body for insertion into and removal from the pocket. One or more resilient support members may be provided for collapsing and expanding the support body and the prosthesis.

Abstract: An apparatus and method of generating a 3D ultrasound image includes acquiring a 3D volumetric data set corresponding to a 3D imaging volume of an ultrasound probe in a 3D detection volume; acquiring a position of the ultrasound probe with respect to the 3D detection volume; acquiring a position of an interventional medical device with respect to the 3D detection volume; determining a position of the interventional medical device relative to the 3D imaging volume of the ultrasound probe; determining an interventional medical device-aligned plane that intersects with a longitudinal axis of the interventional medical device; extracting a texture slice from the 3D imaging volume for a corresponding interventional medical device-aligned plane positional and rotational orientation; mapping the texture slice onto the interventional medical device-aligned plane; and rendering the interventional medical device-aligned plane as a 3D ultrasound image and displaying the rendered 3D ultrasound image on a display screen.

Abstract: A probe cap for use with an ultrasound probe including a head portion and an acoustic surface is disclosed. In one embodiment, the probe cap includes a body that defines a cavity sized for releasably receiving the head portion of the probe therein. The probe cap body further defines a hole that is proximate the acoustic surface of the head portion. A compliant spacer component is disposed in the hole. The spacer component can include a hydrogel and provides an acoustic path between the acoustic surface and a tissue surface of a patient. The spacer component includes a skin contact surface that defines a concavity and is deformable against the tissue surface. Additional embodiments disclose various probe cap and accompanying needle guide designs for use in assisting a clinician with ultrasound probe use and needle insertion into a patient.

Abstract: An introducer used to provide a route through which a catheter or other medical device is inserted so as to gain access to a subcutaneous vessel of a patient is disclosed. The introducer is configured so as to minimize the amount of force needed to enter and dilate a vessel, thus reducing trauma to the vessel and the patient. In one embodiment, an introducer is disclosed, comprising a sheath and a dilator. The sheath includes a tubular portion that defines a lumen. The dilator includes an elongate body and a tapered distal tip and is configured to be removably disposed within the lumen of the tubular portion of the sheath. The dilator elongate body defines a cylindrical recess proximally extending from the tapered distal tip. The cylindrical recess configured to receive therein the tubular portion of the sheath when the dilator is disposed within the tubular portion of the sheath.

Abstract: A surgical fastener is provided for various surgical fastening applications, including attaching an implantable prosthesis, such as a soft tissue repair fabric, to tissue and/or muscle. The surgical fastener may include a coil body and a separate head that is attached to the coil body. The head may include an internal thread that is threadably attached to the coil body. The head may also be further secured to the coil body with a compression fit therebetween. A locking feature may prevent back-out of the coil body from the head. The surgical fastener may be assembled by threading the coil body through the head.

Abstract: An apparatus for performing a medical procedure and, in particular, an aortic valvuloplasty, in a vessel for transmitting a flow of fluid. The apparatus includes an inflatable perfusion balloon including an internal passage for permitting the fluid flow in the vessel while the perfusion balloon is in an inflated condition, the balloon including a plurality of cells in a single cross section and a covering for at least partially covering the cells. A valve associated with the balloon controls the fluid flow within the passage, the valve being arranged external to the passage. The valve may form a tubular extension of the covering, or may be separate from the covering, and may comprise flaps. A spiral covering may also form the valve.

Abstract: A repair prosthetic for repairing a hernia is disclosed. In some embodiments, the repair prosthetic includes a patch body, a frame that assists in spreading the patch body from a reduced configuration to an expanded configuration, and a plurality of tethers attached to the patch body at locations between the frame and a periphery of the patch body. In various embodiments, the tethers can be tensioned to mitigate curling or creasing in the patch body to flatten the patch to facilitate attachment to tissue.

Abstract: A method of operating a biopsy device includes providing a sampling mode for taking a tissue sample with a biopsy needle; providing an insertion/removal mode for inserting or extracting the biopsy needle from living tissue; displacing a primary drive member through a continuous range that defines a first interval and a second interval; transmitting a motive force via the primary drive member to a first drive element during the first interval to cause a pump to generate a vacuum in the biopsy needle; and, transmitting a motive force via the primary drive member to a second drive element during the second interval to change the biopsy needle from the insertion/removal mode to the sampling mode.

Abstract: A virtual tracking system for a virtual medical device. The virtual medical device may include a tangible proximal portion that at least temporarily has a magnetic element attached thereto. The system includes a tracking circuit configured to track movement of the virtual medical device and a display. The tracking circuit may include at least one reception component configured to detect a magnetic field of the magnetic element and to generate magnetic field strength data. The tracking circuit may also include a processor that iteratively computes position data of a virtual distal portion of the virtual medical device according to the magnetic field strength data so as to simulate insertion of the virtual distal portion of the virtual medical device into a body of a patient. The display may be configured to depict an image of the computed position data of the virtual distal portion of the virtual medical device.

Abstract: Provided herein in some embodiments is a catheter including an elongate body with a polymeric portion and a metallic portion; a balloon over at least some of the polymeric portion; a coupler formed over or between the polymeric and metallic portions; and one or more scoring wires. The metallic portion can include a spiral-cut portion configured to prevent elongation and kinking of the elongate body. The one or more scoring wires can be fixed to and extend from a tip at a distal end of the elongate body, over the balloon, through the polymeric portion of the elongate body, through the coupler, and to the metallic portion of the elongate body. The one or more scoring wires can be fixed to an internal surface of the spiral-cut portion or formed from the spiral-cut portion.

Abstract: A blood filter delivery system for delivering a filter into a vein includes an introducer and a push rod with a spline member disposed along the push rod. The spline member has a main body, and first and second boss portions spaced apart along the longitudinal axis to provide a gap for retaining anchor member of the filter during delivery via the introducer.

Abstract: A catheter securement device holds a medical article such as a catheter in position upon the body of a patient and at least inhibits longitudinal movement of the medical article. The securement device includes a retainer and a clamp. The retainer and clamp include interengaging structure. The interengaging structure may be a ratchet mechanism by which a medical provider tightens the clamp against the retainer. The ratchet mechanism allows a single securement system to be used with medical articles that have different longitudinal lengths as well as medical articles that have distally located contact surfaces. The retainer forms a channel into which at least a portion of the medical article is inserted. Each of the retainer and the clamp include at least one abutment surface that can abut against a contact point or surface on the medical article. The abutments inhibit motion of the medical article in proximal and distal directions through the channel when the clamp is tightened against the retainer.

Abstract: An intraluminal prosthesis includes a stent architecture having a series of stent elements repeating along a circumferential axis. One series of stent elements includes v-shaped stent elements having at least four different orientations, and V-shaped stent elements connecting adjacent v-shaped stent elements. One series of stent elements includes R-shaped stent elements having at least four different orientations, and U-shaped stent elements having at least two different orientations, the U-shaped stent elements connecting adjacent R-shaped stent elements. Adjacent series of stent elements can be connected by connectors. Portions of the stent elements may narrow in width along a length thereof. The stent architecture may include radiopaque element receiving members. The stent architecture may be formed by machining a metal or polymer tube. The intraluminal prosthesis may include one or more graft layers.

Abstract: A self-sealing vascular graft, including a substrate with a sealant layer and several optional additional layers, is described. The substrate can be ePTFE and the material used for the sealant and additional layers can be polyurethane. The sealant layer and additional layers may include one or more base layers, one or more foam layers, beading of different sizes and shapes, and ePTFE tape. A flared cuff may be integral to one or both ends of the substrate or may be attached to one or both ends. Various methods of making a self-sealing vascular graft are also described, including methods of disposition, methods of forming, methods of bonding and methods of attaching.

Abstract: An apparatus for performing an endovascular procedure using ultrasonic energy includes a catheter with a proximal end portion and a distal end portion. The distal end portion includes a first window, which may expose a wave guide for delivering the ultrasonic energy for performing the endovascular procedure. A cover may be provided for selectively covering the window. By selectively controlling the position of the sheath, the transmission of ultrasonic energy may be regulated accordingly for providing a desired treatment regimen.

Abstract: A catheter including a core wire, a sonic connector at a proximal terminus of the core wire, and a tip member at a distal terminus of the core wire. The core wire can be at least partially disposed within a lumen of an elongate body. The sonic connector can be configured to couple to an ultrasound-producing mechanism. The tip member can be welded to the core wire at one or more weld locations between the tip member and the core wire, and the tip member can flare from the core wire at one or more weld-free locations between the tip member and the core wire. The manner in which the tip member can flare from the core wire at the one or more weld-free locations is characteristic of ultrasonic activation of the tip member.

Abstract: A biopsy apparatus includes a housing, a biopsy cannula mounted to the housing, and a cannula rotation mechanism mounted to the housing. The cannula rotation mechanism has a thumbwheel, a first gear, and a second gear. The thumbwheel is configured to rotate about a rotational axis, with the rotational axis being perpendicular to the longitudinal axis of the biopsy cannula. The first gear is mounted in fixed attachment to the thumbwheel. The second gear is mounted in fixed attachment to the biopsy cannula. The first gear is in mesh with the second gear such that the first gear is directly drivably engaged with the second gear to rotate the biopsy cannula about the longitudinal axis when the thumbwheel is rotated.