1098 results about "Proximal point" patented technology

An articulation mechanism for a surgical instrument includes an articulation assembly, a plurality of cables, and a trigger. The cables are coupled to the articulation assembly at a proximal end thereof and extend distally therefrom. The cables are configured to engage an end effector assembly of the surgical instrument at a distal end thereof. The trigger is coupled to the articulation assembly and is selectively moveable from a shipping position to a use position. In the shipping position, the cables are substantially un-tensioned. In the use position, the cables are disposed in an initial tensioned position. In the use position, the trigger is moveable between an unlocked position and a locked position. In the unlocked position, the cables are selectively tensionable to articulate the end effector assembly. In the locked position, the tensions on the cables are maintained to lock the end effector assembly in position.

An endoscopic surgical device is provided and includes an endoscopic anchor retaining / advancing assembly including a proximal tube portion and a distal tube portion pivotably connected to one another at an articulation joint; a proximal inner shaft rotatably disposed within the proximal tube portion; a distal inner shaft rotatably disposed within the distal tube portion; and a relatively flexible intermediate drive cable mechanically interconnecting the proximal inner shaft and the distal inner shaft, wherein the intermediate drive cable extends across the articulation joint, wherein the intermediate drive cable defines a central longitudinal axis that is off-set a radial distance from a central longitudinal axis of the proximal tube portion and the distal tube portion.

A device for treating a tissue includes a capsule extending longitudinally from a proximal end to a distal end and including a channel extending therethrough, the capsule releasably coupled to a proximal portion of the device and clip arms, proximal ends of which are slidably received within the channel of the capsule so that the clip arms are movable between an open configuration, and a closed configuration. A core member is coupled to the clip arms, the core member including a proximal portion and a distal portion releasably connected to one another so that, when the core member is subjected to a predetermined load, the proximal and distal portions are separated from one another. An electrically conductive control member is connected to the core member, a proximal end of the connected member connected to a power source for delivering an electrical current to the clip arms.

A prosthetic mitral valve includes a proximal anchor, a distal anchor, and a central portion therebetween. The proximal and distal anchors each include a first outer frame and a second outer frame. The first outer frame includes a plurality of first arcs joined together, and the second outer frame includes a plurality of second arcs joined together. The plurality of first arcs are out of phase relative to the plurality of second arcs.

A lead assembly for an electrical stimulation system includes terminals disposed along a proximal end of a lead body and electrodes disposed along a distal end of the lead body. The electrodes include segmented electrodes. At least one distal marker is disposed along the distal end of the lead body. The distal marker identifies the circumferential position of at least one of the segmented electrodes along the lead body. The distal marker is aligned with at least one of the segmented electrodes along the longitudinal length of the lead body. At least one proximal marker is disposed along the proximal end of the lead body. The proximal marker is aligned with the distal marker along the longitudinal length of the lead body. The distal marker and the proximal marker are discontinuous with one another along the lead body.

There is described a method for determining a mechanical axis of a femur using a computer aided surgery system having an output device for displaying said mechanical axis, the method comprising: providing a position sensing system having a tracking device capable of registering instantaneous position readings and attaching the tracking device to the femur; locating a center of a femoral head of the femur by moving a proximal end of the femur to a first static position, acquiring a fixed reading of the first static position, repeating the moving and the acquiring for a plurality of static positions; and locating the centre by determining a central point of a pattern formed by the plurality of static positions; digitizing an entrance point of the mechanical axis at a substantially central position of the proximal end of the femur; and joining a line between the entrance point and the center of rotation to form the mechanical axis.

A method for performing an open wedge osteotomy, the method comprising:forming a cut in a bone;manipulating the portions of the bone adjacent to the cut so as to open the cut into a wedge-like opening;providing an osteotomy implant, wherein the osteotomy implant comprises:an elongated body characterized by a distal end and proximal end, the elongated body having a screw thread thereon;positioning at least the distal end of the elongated body into the wedge-like opening so that the screw thread engages the surrounding bone; andthreadingly advancing the elongated body into the wedge-like opening until the portions of the bone assume the desired positioning, with the elongated body stabilizing the bone portions in this position.

There is described a method for determining a mechanical axis of a femur using a computer aided surgery system having an output device for displaying said mechanical axis, the method comprising: providing a position sensing system having a tracking device capable of registering instantaneous position readings and attaching the tracking device to the femur; locating a center of a femoral head of the femur by moving a proximal end of the femur to a first static position, acquiring a fixed reading of the first static position, repeating the moving and the acquiring for a plurality of static positions; and locating the centre by determining a central point of a pattern formed by the plurality of static positions; digitizing an entrance point of the mechanical axis at a substantially central position of the proximal end of the femur; and joining a line between the entrance point and the center of rotation to form the mechanical axis.

Catheter having a proximal section and a distal section. The proximal section having at least a delivery lumen and a guidewire receiving lumen, the guidewire receiving lumen having a proximal guidewire exit port at a location proximal of the distal end of the proximal section. A reinforcing tubular member located in the proximal section delivery lumen extending from substantially the proximal end of the proximal section to a point distal to the proximal guidewire exit port, wherein the reinforcing tubular member transitions from relatively rigid to relatively more flexible from a proximal point to a distal point thereon and has an outer diameter equal to about the inner diameter of the delivery lumen for at least a portion of the reinforcing tubular member that extends distal to the proximal guidewire exit port. The distal section having at least a delivery lumen and a guidewire receiving lumen.

Apparatus for performing a transgastric procedure includes an elongated tubular main access device having the first lumen with open proximal end and a side opening distal end, and a second lumen with open ends. A balloon having a wall on the outside of the device surrounds the distal end and a fluid conduit extends along the device for inflating the balloon so that when the device is inserted into a patient's esophagus and the balloon is inflated, the portion of the esophagus opposite the distal end is isolated from the remainder of the esophagus. The apparatus may also include a side access unit having an elongated flexible coaxial inner and outer tubes having proximal and distal ends and being movable relatively in the axial direction. First seals are mounted to the distal end of the outer tube, and second seals are mounted to the distal end of the inner tube, an actuator adjacent to the proxable ends of the tubes move the tubes relatively so as to vary the axial spacing the first and second seals. Various methods for using the apparatus are also disclosed.

A connector is provided for coupling an end of a coaxial cable to a terminal. The connector includes a coupler having an annnular collar, a body member, one end of which includes a deformable lip inserted with elastic deformation through the collar opening, and a post. In a cable-installed position, the post is received in the body member to form an annular chamber sufficiently narrow in the cable-installed position to compress the outer conductor and the jacket for establishing a distal seal. Tightening of the coupler to the terminal compresses the lip between the post flange and the annular collar for establishing a proximal seal.

A method and apparatus of limiting at least one degree of movement between a superior vertebral body, an inferior vertebral body, and an intermediate vertebral body that is disposed between the superior and inferior vertebral bodies of a patient. The method can comprise: advancing a distal end of a stabilization device into a pedicle of the intermediate vertebral body; positioning a proximal portion of the stabilization device such that the proximal portion limits at least one degree of movement between the superior vertebral body and the intermediate vertebral body by contacting a surface of the superior vertebral body; and advancing a distal end of a fixation device into a facet of the intermediate vertebral body and into a facet or pedicle of the inferior vertebral body for stabilizing the intermediate vertebral body and the inferior vertebral body.

An implantable lead adaptor is disclosed that includes an encapsulated thermoplastic housing defining a proximal end portion and a distal end portion. The proximal end portion has a first receptacle configured to receive a first type of connector assembly associated with a first implantable cardiac lead, and a second receptacle configured to receive a second type of connector assembly associated with a second implantable cardiac lead. An elongated flexible lead portion extends from the distal end portion of the adaptor housing. A connector assembly is operatively associated with a distal end section of the flexible lead portion of the adaptor for connection to an implantable pulse-generating device, such as, for example, an implantable pacemaker or defibrillator. Low resistance conductor wires electrically connect the connector assembly associated with the distal end section of the lead portion with the first and second receptacles of the adaptor housing.

A soft tissue anchor device and methods of installing the soft tissue anchor device are disclosed. The device has an elongate body having a proximal end and a distal end. There is a helical anchor on the distal end. A retention structure is provided on the body, proximal to the anchor. The device also includes a proximal anchor, moveably carried by the body. The device includes an adjustable flange that is configured to receive the proximal anchor. The proximal anchor is configured to be rotational with respect to the flange. The adjustable flange is configured to be positioned at a variable angle with respect to the body. The proximal anchor is moveable in the distal direction with respect to the body and the retention structure resists proximal movement of the proximal anchor with respect to the body.

A communication cable is provided that satisfies the requirement of Cat.6 for near-end cross talk wherein the difference between the maximum and minimum values of delay time among the four twisted wire pairs constituting the cable is within 25 ns / 100 m. The communication cable is made by entwining four twisted wire pairs (T1), (T2), (T3), (T4) made by twisting pairs of insulated wires made by covering electrically conductive wires by polyolefin thermoplastic resin with each pair being twisted with a twist pitch different from the others (pitch: P1<P2<P3<P4) and the inter-pair interposer (6) made of polyolefin thermoplastic resin, while being entwined with each wire pair, around a central interposer (2) made of polyolefin thermoplastic resin having cross sectional area of S1. Cross sectional area S1 of the central interposer (2) satisfies the relationship of inequality S1>=[{4.1 d / (1+{square root over (2)})}.0.35]2xpi, while the inter-pair interposer (6) that is entwined with the twisted wire pairs is located at such a position as adjoins the twisted wire pair (T1) having the least pitch P1 and does not adjoin the twisted wire pair (T4) having the largest pitch P4.

A wide angle HDTV endoscope includes at least two optical imaging channels. Lenses close each channel at the distal end of the endoscope. The imaging channels each have a different field of view in complementary directions, and have overlapping or cross-over field of view areas. Received images are transmitted along the longitudinal axis of the imaging channels of the endoscope to a camera head that contains a wide screen image sensing device. An external light source provides the required lighting and an image processing device can provide necessary software algorithms to format the images and to control any overlapping or cross-over field of view areas to obtain a single display image. In another arrangement, optical blocking elements provided at the proximal end of the endoscope or within the imaging channels eliminate portions of one or more images from the imaging channels so that at the cross-over areas only a single image is provided to the imaging device.

A device for implanting into an atrial septum of a patient. In some embodiments, the device has a core region to be disposed in an opening in the atrial septum; a distal retention region adapted to engage tissue on a left atrial side of the septal wall; a proximal retention region adapted to engage tissue on a right atrial side of the septal wall; and a retrieval region comprising a plurality of retrieval members, each retrieval member comprising a connector at a proximal end, the connector being adapted to connect to a delivery system. The device has a delivery configuration and a deployed configuration, the core region, distal retention region and proximal retention region each having a smaller diameter in the delivery configuration than in the deployed configuration, the retrieval member connectors being disposed proximal to and radially outward from the opening in the deployed configuration.

An apparatus for enhancing audibility of a far-end speech signal from a far-end user to a near-end user in a telephony system includes a near-end background noise signal level estimator (26) at the near-end user. A near-end speech signal level estimator (24) is also provided at the near-end user. A gain control logic (22) determines a gain (G) for amplification of the far-end speech signal based on both estimated speech and background noise signal levels.

A needle shield assembly with a needle having a distal tip and a static feature is provided. The needle shield assembly includes an adapter having an open distal terminus and an open proximal terminus to allow passage of the needle and a needle shield slidably associated with the adapter having an open distal end and an open proximal end where the open proximal end is sufficiently narrow to restrict proximal movement of the needle static feature causing the shield to move in a proximal direction when the needle is pulled proximally after the static feature has established contact with the needle shield proximal end. The assembly includes a canting plate having an unactivated first position and an activated second position that restricts needle movement. The canting plate is activated via a canting plate retention system in communication with the canting plate and responsive to proximal movement of the needle.

Catheters, systems, and methods are provided for performing medical procedures, such as tissue ablation, adjacent the ostia of anatomical vessels, such as pulmonary veins. The catheter comprises an elongated flexible catheter body, which includes a proximal shaft portion and a distal shaft portion, and a tracking element carried by the distal shaft portion. The proximal section is pre-shaped to form a curve having an apex sized to be inserted into the vessel ostium, and a distal section configured to contact the adjacent tissue when the curve apex is inserted within the vessel ostium. The method may comprise inserting the curve apex into the vessel ostium to place the distal section in contact with a first tissue site adjacent the vessel ostium, and determining a location of the tracking element(s) within a coordinate system while the distal section is in contact with the first tissue site.

A jointed system for delivering a medical device to a target location within a human anatomy, comprising: a first segment that is a hollow cylinder, wherein a first flange and a second flange are attached to the distal end and extend distally away from the first segment; a second segment that is a hollow cylinder and has a proximal end and a distal end, wherein a third flange and a fourth flange are attached to the proximal end and extend proximally away from the second segment; a connector element having four cylindrical lugs extending radially away from a central point, wherein each lug passes, respectively, through a circular hole, and further wherein the connector element defines at least two separate openings extending in a direction from the distal end of the first segment to the proximal end of the second segment.

A minimally invasive surgical instrument having an elongate stem extending between a proximal end which in use is located externally of an operating space and a distal end which in use is located within an operating space. At least a portion of the stem is malleable to facilitate manipulation of the stem in the operating space and then to maintain the stem in the manipulated position and / or orientation within the operating space. The instrument has an end effector at the distal end of the stem, the end effector having a proximal main body and distal operating means, such as graspers or cutters. The instrument has at least one joint for independent movement of the end effector main body in at least one direction relative to the distal end of the stem for enhanced degrees of freedom of the instrument.

A videoconferencing system has a videoconferencing unit that use portable devices as peripherals for the system. The portable devices obtain near-end audio and send the audio to the videoconferencing unit via a wireless connection. In turn, the videoconferencing unit sends the near-end audio from the loudest portable device along with near-end video to the far-end. The portable devices can control the videoconferencing unit and can initially establish the videoconference by connecting with the far-end and then transferring operations to the videoconferencing unit. To deal with acoustic coupling between the unit's loudspeaker and the portable device's microphone, the unit uses an echo canceller that is compensated for differences in the clocks used in the A / D and D / A converters of the loudspeaker and microphone.

In one embodiment, a process, for fabricating a medical lead comprises: providing a splicing tube having a plurality of angularly spaced longitudinal grooves; placing a first plurality of conductors within the plurality of angularly spaced grooves defined on an exterior surface of the splicing tube; placing a second plurality of conductors within the plurality of angularly spaced grooves and adjacent to the first plurality of conductors such that a portion of the distal ends overlap a portion of the proximal ends; positioning conductive filler material adjacent to the overlapped portions of the distal and proximal ends; electrically coupling the proximal ends of the first plurality of electrodes to respective proximal ends of the second plurality of electrodes; molding insulative material about at least the electrode assembly and the splicing tube; and fusing the splicing tube with the insulative material from the molding and the lead body.

An occlusion device suitable for endovascular treatment of an aneurysm in a blood vessel in a patient, including a substantially tubular structure having a proximal end region and a distal end region, having a first, expanded condition and a second, collapsed condition. The device has dimensions in the second, collapsed condition suitable for insertion through vasculature of the patient and through a neck of the aneurysm. The device further includes a control ring having a substantially annular body disposed on the proximal end region of the structure and at least substantially circumscribing the proximal end region to prevent radial expansion of the proximal end region and to provide an engagement feature during manipulation of the occlusion device.

A staple for attaching a sheet-like implant to tissue or bone may, include first and second arms, and first and second flukes. In some embodiments, the first arm has a proximal end and a distal end, and the second arm has a proximal end and a distal end. A bridge extends from the proximal end of the first arm to the proximal end of the second arm. The first fluke has a proximal end abutting the distal end of the first arm, and the first fluke extends distally from the first arm. The first fluke has a lateral extent larger than a lateral extent of the first arm and is mounted eccentrically thereto. The first fluke includes a proximal surface projecting at an outward angle in a proximal direction away from the distal end of the first arm to engage the tissue or bone when inserted therein. The second fluke has similar features. This arrangement causes the first and second flukes to rotate in response to a pullout force on the bridge. Methods for attaching a sheet-like implant to a target tissue are also disclosed.

A systems and methods for controlling temperature in a cryogenic device includes providing a device having a probe and a heater element. A distal region of the probe is engaged with the target region. Measuring and recording current temperature of a proximal region of the probe and time of the measurement is used to determine slope of a temperature curve defined by two points. The first point is defined by the current temperature and time of measurement and a second point is defined by a previous measurement of proximal region temperature and time of measurement. When the slope is less than a slope threshold value a treatment flag is activated, treatment start time is recorded and the proximal region is heated with the heater element. Heating is discontinued and the treatment flag is deactivated after elapsed treatment time exceeds a duration threshold value.

A near end point of presence (PoP) of a cloud proxy service receives, from a client device, a request for a network resource. A far end PoP from a plurality of PoPs of the cloud proxy service is identified. Responsive to determining that a version of the network resource is stored in the near end PoP, a request for the network resource is transmitted to the far end PoP with a version identifier that identifies that version. The far end PoP receives, from the near end PoP, a response that includes difference(s) between the version of the network resource stored in the near end PoP with a most current version of the network resource. The response does not include the entire network resource. The near end PoP applies the specified difference(s) to the version that it has stored to generate an updated version of the network resource, and transmits it to the client device.