Abstract: A cannula (10) receives surgical instruments (120) for performing a surgical procedure on a body (130). The cannula (10) comprises a tube structure (12) defining a passage (16) through which the surgical instruments (120) are inserted into the body (130). The tube structure (12) has a proximal end (20) and a distal end (62). The tube structure (12) includes an expandable portion (40) for enabling an increase in the cross-sectional area of the passage (16) at the distal end (62). The expandable portion (40) of the tube structure (12), when expanded, has a conical configuration.

Abstract: A medical electrical lead implant tool includes a gripping assembly, terminating a distal end of an elongate shaft, adapted to alternately grasp the lead and release the lead and to rotate the lead, and a user control terminating a proximal end of the shaft. An internal drive cable extends within the shaft coupling the gripping assembly to the user control. The user control facilitates single-handed manipulation of a slidable dial, which may be grasped by fingers of a hand for longitudinal and rotational manipulation when a stationary handle is held in a palm of the hand; the longitudinal manipulation causing the gripping assembly, via the drive cable, to alternately grasp the lead and release the lead and the rotational manipulation causing the gripping assembly, via the drive cable, to rotate the lead.

Abstract: An insertion guide is shown that includes at least one insertion point adjustment device. A user such as a surgeon is able to adjust a lateral position of an insertion point to more precisely center the insertion point within an opening in a subject, such as a burr hole. Selected insertion guide devices further include a centering guide that easily indicates to a user when the insertion point is substantially centered within the opening in the subject. Selected insertion guide devices include adjustability of multiple degrees of rotational freedom of an insertion axis. Selected insertion guide devices further permit a user to fix multiple degrees of rotational freedom of an insertion axis using a single locking device. Tissue damage due to an attachment procedure of an insertion guide device is reduced using selected configurations described herein.

Abstract: A delivery system for delivering an endoluminal implant to a distal deployment location inside a body lumen from a proximal access location outside the lumen. The system comprises the implant, a catheter, and a slidable sheath having an advanced position in which the sheath covers the implant and a retracted position in which the implant is exposed. The catheter comprises a stabilizer having a distal end adjacent the implant proximal end and/or a catheter tip attached to a central core slideably disposed relative to the implant and having a proximal end adjacent the implant distal end. The catheter tip proximal end and/or the stabilizer distal end comprises a docking section adapted to releasably engage a portion of the implant. Each docking section has an engagement geometry comprising a flared engagement surface that extends inside a short axial length of the implant or a pocket having a bottleneck geometry.

Abstract: Systems and methods for crossing stenosis, partial occlusions, or complete occlusions within a body lumen. The systems generally include an elongate member such as a hollow guidewire that houses a rotatable and translatable drive shaft. The drive shaft typically has a distal portion that is advanced to create a path in the occlusive material that is large enough to allow the hollow guidewire to cross the occlusive material.

Abstract: A device is disclosed for assisting surgical operations inside a vessel, particularly for the minimally invasive explantation and implantation of cardiac valves, comprising an operating structure adapted to be implanted within the vessel, that is adapted to be fixedly and detachably joined to the inner wall of the vessel and is provided with at least one connector and/or support structure for a further instrument required for the surgical operation.

Abstract: A filter device is adapted to function as a guidewire, an exchange guidewire, and provide embolic protection during a procedure. The filter device includes a filter assembly that is either integral with or coupled to a guide member. The filter assembly includes a plurality of struts that expand outwardly to deploy a filter that collects or captures material flowing along the blood vessel within which the filter device is deployed. The plurality of struts are constrained by a restraining member or mechanism that prevents the plurality of struts from expanding or extending outwardly to deploy the filter. Cooperating with the restraining member or mechanism is an actuating assembly that is adapted to release the restraining member or mechanism and enable the filter to be deployed from the guide member. A capture catheter is cooperates with the filter device and substantially surrounds the filter during removal of the filter device.

Abstract: The invention concerns a reinforcing implant for tissue sutures used for mechanically reinforcing stitched tissue zones, and consisting of a textile lap based on polyuronic acid or one of its salts

Abstract: An ultrasonic surgical instrument for dissection and coagulation of tissue is provided. The surgical instrument includes a vibration coupler supported within a housing and operably connected to an ultrasonic generator. An angled blade member is connected to the distal end of the vibration coupler to conduct high frequency vibration from the ultrasonic generator to the blade member. A clamp member is positioned adjacent to the blade member and is movable from a first position to a second approximated position. The clamp member and angled blade member combine to enhance contact between the tissue and the blade member during operation of the instrument to improve the performance of the instrument.

Abstract: The present invention provides an infant teething gel applicator for the application of anesthetic gel, having a teething portion to administer a regulated and minimal dosage of medication, and a collar to fit inside a standard baby bottle. The collar extends radially in a first plane and the teething portion extends laterally from the collar and is aligned longitudinally in a direction generally orthogonal to the collar. The teething portion has an outer engaging surface with a plurality of protrusions extending outward therefrom. Each individual protrusion contains a single minute pore configured to harbor medication, which is dispersed upon an infant chewing the device.

Abstract: A tissue removal method utilizes a tool having a shaft with a flexible inner member rotatable about the shaft and an outer member extending along the inner member. The inner and outer members are bent to a desired configuration and the inner member rotates relative to the outer member while maintaining the shaft in the desired configuration under the influence of the rigidity of the outer member during rotation of the inner member. A patient's body tissue is cut with a cutting element connected with the inner member during rotation and the body tissue cut from the patient is moved along a passage within the shaft while the shaft is maintained in the desired configuration.

Abstract: A deformable sheath is attached to a catheter and introduced intravascularly to be expanded against an arterial wall and entrap plaque therebetween. A stent is subsequently deployed within the expanded sheath and the sheath is then withdrawn from within the vasculature to leave the stent expanded against the arterial wall with the plaque entrapped therebetween.

Abstract: A surgical instrument includes an elongate hollow probe having first and second apertures (4 and 5) at its distal end portion. An elongate drive shaft disposed within the probe (1) and mounted for rotation about its longitudinal axis within the probe. A cutting tool (2, 34) is located at the distal end of the drive shaft, and is positioned adjacent to the first aperture (4). A bipolar electrosurgical device (3) is located at the distal end of the probe (1) in the region of the second aperture (5). The electrosurgical device includes an active electrode (13) and a return electrode (11) separate and insulated therefrom. A motor (6) is provided for rotating the drive shaft; and suction means is provided for selectively providing a source of suction at either the first apertures (4) or the second aperture (5).

Abstract: A force applying surgical system is provided for use to assist in the insertion and/or removal of a surgical tool or a device attached thereto from an orthopedic structure. This surgical system comprises a medical impacting device that mates with a surgical tool such that the impacting device can be manually reciprocated along an axis of the tool to forcefully impact the impacting device on a portion of the tool. The impacting device can generate a distally directed force for inserting the tool (and/or an attached device) into an orthopedic structure, or it can generate a proximally directed force to remove the tool (and/or attached device) from an orthopedic structure.

Abstract: An expandable bifurcated stent comprising a proximal end and a distal end in communication with one another. The proximal end comprises a primary passageway and the distal end comprises a pair of secondary passageways. The stent is expandable from a first, contracted position to a second, expanded position upon the application of a radially outward force exerted on the stent. Each of the primary passageway and the secondary passageway being constructed of a tubular wall having a porous surface, a method for production of a bifurcated stent is also described. The method comprises the step of connecting a first stent section to a second stent section, the first stent section having an end thereof adapted for connection to an opening disposed along the length of a second stent section.

Abstract: A method of performing a surgical procedure on a body includes providing a cannula having a tubular structure with first and second tubular portions defining first and second passages for receiving surgical instruments. The second tubular portion is inserted inside the body and the first tubular portion is inserted so that the first tubular portion extends from an exterior of the body to inside the body. The second tubular portion expands to increase the cross-sectional area of the second passage in the second tubular portion while the second tubular portion is inside the body. The cross-sectional area of the first passage in the first tubular portion is maintained. The first tubular portion has a first thickness and the second tubular portion has a second thickness different than the first thickness.

Abstract: The present invention includes a coiled wire formed of a shape memory material for implantation into an anatomical defect. After implantation of one or more of the coiled wires according to the present invention, the defect is occluded and thereby corrected or treated. Prior to implantation, the coiled wire is generally elongated and thereafter it reverts to a predetermined shape that is suitable for occluding the defect. At least one clip having at least two prongs may be provided on the wire for attachment to body tissue. Preferably the wire is made of nickel-titanium. In an alternative embodiment, the coil includes a plurality of layers. At least one of these layers is formed of a shape memory material.

Abstract: The present invention relates to an apparatus and a method for sealing a puncture in a tubular tissue structure or the wall of a body cavity. More specifically, the present invention is directed to an apparatus and method for sealing a puncture site in the wall of a tubular tissue structure, or in the wall of a body cavity with submucosal tissue or another extracellular or matrix-derived tissue capable of remodeling endogenous connective tissue in vivo. The submucosal tissue or another extracellular matrix-derived tissue is inserted into the puncture site as a sheet on an introducer element such as a needle, a cannula, a guide wire, an introducer element adapted for dialysis, an introducer element adapted for catheterization, a trocar, or any other introducer element used to access the lumen of a tubular tissue structure or used to access a body cavity.

Abstract: The present provides a removable vessel filter comprising a first and second filtering portion and a first and second anchoring portion, wherein a transverse dimension of the first filtering portion in an expanded configuration is less than a transverse dimension of the first anchoring portion in an expanded configuration, and a transverse dimension of the second filtering portion is less than a transverse dimension of the second anchoring portion. The first and second filtering portions are positioned closer to each other than the first and second anchoring portions, and the anchoring portions being formed on first and second opposite portions of the vessel filter. The vessel filter is removable from a vessel wall by engagement of either the first filtering portion or the second filtering portion.

Abstract: The invention relates to an osteosynthetic anchoring member comprising a longitudinal shaft extending along a longitudinal axis having a front shaft portion and a rear shaft portion, the front shaft portion insertable into a bone and comprising anchoring means for fixating the shaft in the bone and the rear shaft portion comprising anti-rotation means for permitting the rear shaft portion to be received in an implantable bone plate or a connecting member and to be secured against rotating about the longitudinal axis. The anchoring means are capable of being extended orthogonally with respect to the longitudinal axis of the shaft, and the rear shaft portion comprises tension means for extending the anchoring means to enable the anchoring member to be fixated within the bone.