87results about How to "Facilitate insertion" patented technology

An apparatus for sealing a passage through tissue includes an elongate shaft and a cylindrical plug disposed on a distal end of the shaft, the plug including a helical thread on its outer surface. Intestinal submucosa may be secured to the plug, e.g., in a cavity in its distal end, that may be delivered into the passage. Alternatively, the plug may be formed from a bioabsorbable material and may be released from the shaft within the passage. The plug is threaded into the passage, thereby engaging the tissue to seal the passage. The shaft is rotated until it engages a blood vessel within the tissue while monitoring blood flow through the vessel. The shaft is rotated to thread the plug into the passage until blood flow ceases through the vessel, whereupon rotation of the shaft is reversed to back the plug until blood flow through the vessel resumes.

An access port for use in laparoscopic surgery is disclosed. The port includes a duct having a one-way valve and a tubular seal. The one-way valve has opposed surfaces that co-apt in response to internal pressure within the duct. The tubular seal has an inner layer with a low friction coefficient surrounded by an outer elastic layer that biases the inner layer into sealing engagement with a surgical tool inserted through the duct. The one-way valve seals the duct in the absence of a tool extending through the duct. The low friction coefficient of the inner layer facilitates insertion and removal of the tool through the duct. The port has a distal end insertable into a pressurized cavity, and a proximal end that extends from the cavity and provides access thereto.

The present disclosure concerns embodiments of an introducer that is adapted to facilitate insertion of a prosthetic device, such as a prosthetic heart valve, into a patient's vasculature. In one embodiment, the introducer comprises an elongated body defining a central lumen extending between distal and proximal ends of the body. The introducer body can also have a longitudinally extending gap extending along the length of the body between the distal end proximal ends. The gap in the introducer allows a user to place the introducer around implant sutures by passing the sutures through the gap and into the central lumen. Similarly, the gap allows the introducer to be easily removed from the sutures and / or a delivery device by passing them outwardly through the gap.

Instruments for use in minimally invasive carpal tunnel release include a cannula and a cutting member movable longitudinally within the cannula to advance a cutting blade of the cutting member along a longitudinal slot in the cannula to sever a transverse carpal ligament disposed over the slot. A dilating member is provided for creating a subligamentous space to accommodate the cannula and / or for removing adhered synovium from a lower surface of the ligament. A method for minimally invasive carpal tunnel release involves establishing a subcutaneous pathway to the carpal tunnel from an incision in the forearm, introducing the cannula in the carpal tunnel via the pathway, and severing the transverse carpal ligament with the cutting blade of the cutting member, all of which steps are performed under direct endoscopic visualization.

An intervertebral implant has two U-shaped inserts set over each other with a center piece in between. The two inserts each have an opposing base surface, two lateral side surfaces, and a contact surface. The contact surface has a channel configured to receive a spinal process of a vertebral body. The center piece has two resting surfaces corresponding respectively to each contact surfaces. The contact and resting surfaces each have corresponding structures that can engage each other such that the U-shaped inserts can each be fastened in a detachable manner to the center piece. The U-shaped inserts each have on the same lateral side surface connecting means to fasten the inserts to gripping elements of a surgical instrument. And the first and second structures can be engaged or disengaged only by the lateral side surface fitted with the connecting means.

Devices and methods for protecting the neurovascular structures about the vertebral column are provided. One embodiment of the invention comprises a neuroprotective stent or device adapted for placement in an intervertebral foramen of a vertebral column and configured to resist compression or impingement from surrounding structures or forces. The stent or device may further comprise a flange or hinge region to facilitate attachment of the device to the vertebrae or to facilitate insertion of the device in the foramen, respectively.

A surgical access apparatus includes an access member dimensioned for insertion within tissue and having a longitudinal opening to permit introduction of a surgical object through the access member to perform a procedure on underlying tissue. A seal member is mounted across the longitudinal opening of the access member and has an internal portion defining an aperture for forming a substantial seal about the surgical object introduced through the longitudinal opening of the access member. The seal member includes a first seal portion extending from the internal portion and being mounted in suspended relation to the access member, and a second seal portion extending from the internal portion and disposed radially outward of the first seal portion, and being attached to the access member

A catheter introducer includes a tube having a proximal end, a distal end and a lumen extending therethrough along a longitudinal axis of the tube for accommodating a catheter traveling along a longitudinal axis of the tube and a head portion coupled to the distal end of the tube. The head portion includes an aperture in fluid communication with the lumen at a proximal end thereof and a tip at a distal end thereof, an exterior surface extending from the proximal end thereof to an opening of the head portion along a first portion of the head portion and extending from the proximal end thereof to the tip along an opposing portion of the head portion and an interior surface extending from the aperture to the opening of the head portion along the first portion of the head portion and extending from the aperture toward the tip along the opposing portion of the head portion. The exterior surface circumferentially tapers from the proximal end to the distal end and the interior surface forms a channel for receiving a catheter passing through the lumen and the aperture, the channel being concave along at least one axis.

Intervertebral disc nucleus replacement implants and methods are provided. The nucleus replacement implant, which is configured to reside within an intervertebral disc nucleus space, includes a core support structure, including a rotatable member and multiple vertebral support structures. The vertebral support structures are disposed in spaced relation with the rotatable member positioned therebetween. The implant further includes an elastic body at least partially surrounding the core support structure. When the rotatable member is in the first orientation, the implant is in a compressed height configuration to facilitate insertion of the implant into the intervertebral disc nucleus space, and when the rotatable member is in the second orientation, the implant is in an extended height configuration to facilitate use of the implant as a prosthetic intervertebral disc nucleus replacement.

This present invention generally relates to devices and methods for repairing an aperture in a biological tissue. In certain embodiments, the invention provides a system for closing an aperture in a biological tissue including a handle, an elongate shaft connected to the handle, and a deployment scaffold connected to the shaft, in which the scaffold is configured to releasably retain a surgical implant and the scaffold is configured to deploy and attach the surgical implant to the biological tissue.

A serviceable safety clip for retaining an automotive trim panel to an inner panel. The serviceable safety clip includes a pin secured to the trim panel, wherein the pin includes a plurality of blades that each include a low retention detent and a high retention detent. The serviceable safety clip also includes a receiver that is secured to the inner panel, wherein the receiver includes an angled face to facilitate insertion of the pin detents and a holding face that retains the pin detents.

An apparatus for displaying merchandise, the apparatus having a base, a pole, and a means for securing the pole in a substantially vertical orientation on the base. A sign holder is preferably attached to an upper end of the pole. A bracket member is preferably secured adjacent the upper end of the pole. The bracket member has at least one prong for supporting one or more sets of disposable receptacles for umbrellas. The means for securing is preferably an insert detachably engaged within a generally cylindrical opening of the base. The insert comprises a generally cylindrical body having a generally cylindrical opening passing through at least an upper portion thereof. A plurality of longitudinal ribs extend radially outward from the body. Outer longitudinal edges of the ribs are sized to tightly abut against the generally cylindrical opening of the base to thereby maintain the insert in a substantially vertical orientation relative to the base. A portion of each of the ribs of the insert preferably taper toward a lower end of each of the ribs for facilitating insertion of the insert into the opening in the base.

An isotope seeding system that controls the release of radioactive seeds for treatment of cancerous cells during cancer treatment procedures. The isotope seeding system comprises at least one seed that is chargeable with radioactive isotopes. At least one dissolvable web netting may alternatively be positioned about the at least one seed, and a seed deployment assembly is utilized for delivering the at least one seed, with or without the dissolvable web netting, into an organism's tissue, to surround cancerous cells. The seed deployment assembly includes an elongated cannula, a hub assembly and an obturator. The hub assembly includes an initial inner diameter at its proximal end and an operable length between the proximal end of the hub assembly and the proximal end of the cannula, the ratio of the initial inner diameter relative to the operable length being in the range of 0.075 to 0.175, to preclude against jamming of the at least one seed, with or without the at least one dissolvable web netting wrapped thereabout, within the hub assembly and / or to further preclude against inadvertent migration of such seeds from the web netting when such netting is utilized.

The present invention relates to an endoscope having a motorized assembly to control the distal end of an endoscope. Preferred embodiments can include disposable and reusable components. The system reduces the force need to control the tip of the endoscope and thereby reduce the risk of perforation′.

A method of installing a safety railing in a building under construction by providing post supports comprising open-topped post sockets on socket supports, mounting the post sockets on a concrete floor formwork with the post sockets spaced above the concrete floor formwork by the socket supports and casting concrete to form a concrete floor on the concrete floor formwork and thereby embedding the post supports in the concrete floor with the concrete extending beneath the post sockets. The lower ends of posts are then inserted into the post sockets to support the posts above the concrete floor and rails are supported on the posts.

A bracket to attach a scaffold support to a vertically oriented stud is disclosed in one aspect of the invention as including a backing member to contact the back surface of a stud; a pair of side members rigidly connected to the backing member and extending along the sides of the stud beyond the front surface of the stud; a connection mechanism to attach the scaffold support to the side members; and a fastening mechanism to attach the bracket to the stud. In certain embodiments, the fastening mechanism includes offset flanges extending from the side members in substantially opposite directions to preclude interference between fasteners passing through the flanges.

A lead fixation tool includes a tapered opening for receiving and guiding a stylet into a lead. The fixation tool also includes an engagement mechanism for gripping a portion of the lead connector so that rotation of the tool causes rotation of an active fixation tip, such as a helical tip, coupled with the lead.

An apparatus for treating urinary incontinence, comprising: a node; a support section adapted for providing urethral support attached to the node; and, an anchoring section adapted for resisting movement of the apparatus attached to the node opposite the support section. Optionally, the support section is adapted to treat incontinence according to at least one of: SUTFS, colpo-elevation or colpo-distension.

Edible animal chew and method of using the animal chew. The animal chew is edible and is configured to clean laniaries and gum tissue of an animal as the animal chews and eats the animal chew. The animal chew comprises all-natural ingredients and is, therefore, free of synthetic ingredients and unhealthy added ingredients, such as added sugars. The animal chew may further contain all-natural vitamins for improving health of the animal. A plurality of first projections and second projections on a proximal end portion and a distal end portion, respectively, are provided to clean laniaries and gum tissue for reducing risk of tooth decay and periodontal disease. A plurality of raised nodules is also provided on the distal end portion for massaging gum tissue to reduce risk of periodontal disease.

Disclosed is an expandable percutaneous sheath, for introduction into the body while in a first, low cross-sectional area configuration, and subsequent expansion to a second, enlarged cross-sectional configuration. The sheath is maintained in the first, low cross sectional configuration by a removable tubular restraint. In one application, the sheath is utilized to introduce a formed in place orthopedic fixation rod such as for use in spinal fixation procedures.

A portable media device includes a memory, a data interface port communicatively coupled to the memory, and a portable housing encasing the memory and data interface port. The portable housing may include a locking retaining portion such as a carabineer clip or the like that locks the media device to a desired article. In certain example embodiments, the portable media device may be a digital camera, an MP3 player, a pocket flash memory or other similar digital devices.

There is provided an endoscope system which can secure appropriate bending stiffness of an insertion portion while maintaining the slide length of an endoscope insertion portion. According to one aspect of one of the present invention, in an endoscope system including an endoscope and an insertion assisting tool in which the endoscope is inserted and which assists the insertion of an endoscope insertion portion into a body, a flexible portion of the endoscope insertion portion includes a projection region which projects from the distal end opening of a tube body when the endoscope insertion portion is located in the distal end position in a movable range with respect to the tube body of the insertion assisting tool, and the projection region includes a bending stiffness change portion in which bending stiffness increases from a first position on the distal end side to a second position on the proximal end side.

A kinetic anchoring deployment system utilizing a high-impulse, high-velocity anchor launching mechanism is described herein. The assembly generally has a handle, a flexible elongate body, and a launch assembly thereupon. The launch assembly uses a number of different mechanisms for creating a high-impulse shock wave for launching a carriage carrying a tissue anchor, e.g., combustible materials, rapid vaporization of a fluid, hydraulic energy transmission, laser energy, compression springs, electromagnetic energy, etc. The deployment system may be advanced intravascularly and / or intraluminally within a patient body for treating a number of different indications.

A spinal implant device for placement between vertebral bodies includes a housing, at least one screw member in the housing, and at least one drive shaft operably engageable with the screw member. The housing includes a first shell member and a second shell member. At least the first shell member has step tracking comprising a plurality of individual riser members for receiving the at least one screw member. The height of the plurality of individual riser members may change along the step tracking. The drive shaft may be operable to rotate the at least one screw member, causing the at least one screw member to move on the plurality of individual riser members. The at least one screw member comprises an external helical thread having a thickness configured to fit in the gaps between adjacent individual riser members, and is engageable with the first and second shell members, whereby the first and second shell members move relative to each other in response to the rotation of the at least one screw member to effect an expansion of the housing or a contraction of the housing from the expansion by reversing the rotation of the at least one screw member.

An insulin infusion system is provided with a manual insertion device having a dual retraction spring (230) configuration for automatic introducer needle (222) retraction. A button (200) of the insertion device is used to insert the introducer needle (222) and catheter (202), and once the introducer needle (222) and catheter (202) have been fully inserted, a rotating engagement releases the dual retraction springs (230) such that the introducer needle (222) automatically retracts, leaving the catheter (202) in the body of the user. An end of the introducer needle (222) remains in the inserted catheter (202) and / or in the septum (206) of the inserted catheter (202) to provide an uninterrupted fluid path.

A beverage maker is disclosed with a removable filter carrier, a receiver for the removable filter carrier, and a locking mechanism to selectively secure and seal the carrier to the beverage maker by way of lifting the carrier to engage a sealing surface. In use, the filter carrier is linearly inserted into the receiver via a front face of the beverage maker. The receiver may also include the locking mechanism. The locking mechanism includes a lever that is actuated to operate the locking mechanism. Actuation of the lever is translated to lift and clamp the filter carrier against the seal surface. In the ‘sealed’ position, the lever is selectively fixed in place until the user actuates the lever so as to release the filter carrier. In the ‘released’ position, the filter carrier is still supported by the locking mechanism but it may be selectively removed from the receiver. The locking mechanism reduces or eliminates conventional issues with securing a filter carrier to a beverage maker such as properly aligning the filter carrier so that it may be secured to the beverage maker, the filter carrier disengaging from the beverage maker during use, or not being able to remove the filter carrier after a brew cycle.

An airway management device such as, for example, an nasal airway management device with inflatable supraglottic laryngeal cuff is provided. The airway management device includes an airway tube, an inflatable cuff, and an inflation passage. The airway tube defines a lumen extending between a proximal end and a distal end. At least the distal end of the airway tube is configured to be inserted through a patient's nasopharyngeal passageway. The inflatable cuff is attached at or near the distal end of the airway tube and defines an opening fluidly coupled with the lumen of the airway tube. The inflation passage may extend along the airway tube and may be coupled to the inflatable cuff to allow inflation and deflation thereof. When in a deflated state the inflatable cuff may be inserted through the patient's nasopharyngeal passageway. When in an inflated state the inflatable cuff may expand to form a seal around the patient's supraglottic laryngeal inlet. A method for utilizing the airway management device to manage a patient's airway may also be provided.