Abstract: A device for artificial insemination, wherein the device includes a dildo member having an internal channel for receiving a tubing connected to a pumping mechanism and associated pumping arm, wherein fluid may be drawn into the dildo member through the pumping mechanism and discharged through the internal tubing at a distal end.

Abstract: This catheter comprises a tubular catheter body defining a longitudinal channel, the distal end of the catheter body being closed, and the channel opening out through a single side orifice onto an external surface of a side wall of the catheter body at a distance from this distal end. The channel includes a curved distal end segment and has a substantially constant diameter along the entire length thereof.

Abstract: A method of stimulating bone regeneration in a discontinuous section of a long bone in a subject requiring same, comprising the step of applying to said discontinuous section of the bone an effective vacuum for an effective length of time. A device for carrying out the method consisting of a sealable tubular-shaped sleeve or cuff that fits snugly and sealably around the bone section to be treated and that can be evacuated via a port that is integral to the sleeve or port.

Abstract: External fixation techniques for immobilizing joints or fractured bones are described herein. An external fixation system may include one or more clamp assemblies connected to one or more rod assemblies at polyaxial joints. Each rod assembly may be length adjustable, and may include a one-way locking mechanism to provisionally lock the length of the rod assembly, and additional locking mechanisms to permanently lock the length of the rod assembly. The system may be deployed pre-assembled as a unit to immobilize a joint or fracture. Another external fixation system further includes a spanning member extending transverse to the rod assemblies. Two or more external fixation systems may be deployed in a stacked configuration on one set of bone pins to immobilize two joints and/or fractures. The systems may be provided in kits including guiding instrumentation, bone pins and pin clamping assemblies for connecting the bone pins to the external fixation systems.

Abstract: Devices for the fixation of a bone fracture and methods of using the devices are provided. The devices comprise at least one distal pin assembly configured to engage a first bone fragment, at least one proximal pin assembly configured to engage a second bone fragment, and a rail bar system configured to connect the distal and proximal pin assemblies together across the bone fracture. Each pin assembly includes a screw portion having a distal end configured to engage first bone fragment and a proximal end, a support sheath portion having a distal end configured to engage the first bone fragment, wherein the support sheath portion defines an elongated channel in which the proximal end of the screw portion is disposed, and a cap portion configured to attach the proximal end of the screw portion to the support sheath portion.

Abstract: A spontaneous-extending and anti-rotation scoliosis correcting system comprises pedicle screws and a plurality of correcting rods locked with the pedicle screws. Each correcting rod includes at least one sleeve and at least one inserting rod which can be inserted into the sleeve. The inner wall of the sleeve and the inserting rod are the same in shape and are in clearance fit. A positioning mechanism for restricting the relative rotation of the inserting rod with respect to the sleeve is arranged on a matching surface between the inserting rod and the sleeve. The scoliosis correcting system has the benefits of ensuring the lateral stability and the anti-rotation function for scoliosis correction; having the performance of spontaneous extending along the growth direction of the spine; and ensuring both the short-term operating effect and the long-term curative effect.

Abstract: A spinal buttress plate includes a body having a top surface and a bottom surface and including an annular lip, a ledge, and a pair of teeth. The annular lip defines an opening. The annular lip and the opening are adapted to engage a screw for facilitating the securement of the buttress plate to one or more vertebrae. The ledge defines an aperture. The ledge and aperture are adapted to engage an instrument for positioning the buttress plate adjacent a spinal bone graft. The teeth are disposed in spaced-apart relation on the bottom surface of the body and are positionable within the one or more vertebrae.

Abstract: In some embodiments, a method comprises disposing a portion of a flexible fastening band into contact with a first bone portion and into contact with a second bone portion. The portion of the flexible fastening band having a substantially uniform shape configured to substantially compliment a shape of the first bone portion and a shape of the second bone portion. The method further includes inserting the portion of the flexible fastening band into a fastener and advancing the portion of the flexible fastening band through the fastener until the first bone portion and the and the second bone portion are stabilized.

Abstract: A medical apparatus for use proximate a surgery location on a spine of a subject includes a first lateral support member and a second lateral support member, each lateral support member coupled to a portion of the spine proximate a first vertebra. A transverse connection member has a first end, a second end, and an intermediate portion therebetween, with the first end coupled to the first lateral support member and the second end coupled to the second lateral support member. A first extension member has a first end and a second end, with the first end coupled to the intermediate portion of the transverse connection member, and the second end coupled to a spinous process of a second vertebra.

Abstract: An adjustable spine distraction implant alleviates pain associated with spinal stenosis and facet arthropathy by expanding the volume and/or cross sectional area in the spinal canal and/or neural foramen. The adjustable implant provides a spinal extension inhibitor. The implant includes elliptical or oval shaped adjustable member or spacer for positioning between and adjustably spacing apart the spinous processes.

Abstract: An osteosynthesis plate according to the invention has at least two legs, which are spaced apart and interconnected by at least one bridge element. The legs each have a certain length and extend in the longitudinal direction from an epiphyseal to a diaphyseal end of the osteosynthesis plate. Moreover, each leg has at least one opening for holding an anchoring element. The size and shape of the bridge element and the legs are configured such that the legs may be applied on both sides of a bone in the region of a joint, preferably on the olecranon.

Abstract: A device and method for fixation of bone fractures has a bone screw comprising a shank with a threaded end portion, on the outer surface. The screw has a through bore with two bore portions differing in diameter. A step in the diameter is formed between these bore portions and is located within the end of the screw having the thread. This step in diameter can support a metal insert which in turn supports a polymer pin when the latter if pressurized with a sonotrode in the bone screw. Together with an applied ultrasonic vibration the pressure fluidizes the polymer pin and presses the material through holes configured in the wall of the bone screw and into surrounding bone.

Abstract: The invention relates to an osteosynthesis pin, in particular for a fracture of a calcaneum, made up of a generally cylindrical hollow body comprising an axial bore extending over the entire length thereof, a plurality of through-holes staggered longitudinally relative to one another and intended for attachment screws to pass therethrough, and at least one oblong opening suitable for an ancillary instrument to pass therethrough for repositioning fractured bone fragments.

Abstract: A system for forming an implant to stabilize an interior of a vertebral body is provided. The system includes a delivery cannula. A plurality of elements are disposed adjacent to one another in the delivery cannula with void spaces defined between the elements. A fluent material, capable of setting to a hardened condition, is disposed within at least a portion of the void space in the delivery cannula. A push rod is movably disposed within the delivery cannula to apply a force to move the elements through the delivery cannula and into the interior of the vertebral body. Upon application of the force, the elements simultaneously carry the fluent material through the delivery cannula and into vertebral body to delivery the fluent material at a low pressure. The fluent material sets to the hardened condition to secure the elements and form the implant.

Abstract: A modular impactor head includes a load transfer member, a base, and a locking assembly. The base defines a space sized and configured to receive the load transfer member therein and to constrain movement of the load transfer member relative to the base in a plurality of directions. The locking assembly is sized and configured to constrain movement of the load transfer member with respect to the base in at least one direction such that the load transfer member is fixed to the base.

Abstract: An intravascular catheter for peri-vascular or peri-urethral tissue ablation includes multiple needles advanced through guide tubes which may be supported by an expandable balloon. The guide tubes expand with open ends around a central axis to engage the interior surface of the wall of the renal artery or other vessel of a human body allowing the injection an ablative fluid for ablating tissue, or nerve fibers in the outer layer or deep to the outer layer of the vessel, or in prostatic tissue. The diameter of the inflated balloon is less than the inside diameter of the vessel, allowing perfusion across the inflated balloon and guide tubes.

Abstract: An improved cryosurgical system for application of medical-grade liquid nitrogen to a treatment area via a small, low pressure, open tipped catheter. The system includes a console, including a touch panel computer, a cryogen module, a suction module and an electronics module, all packaged in a mobile cart, and a disposable spray kit. Improved features include optional low cryogen flow setting to reduce the cryogen flow rate by 50%, improved cryogen flow consistency reducing pressure pulses and peaks (improved sensors, control systems, and control algorithms), an integrated suction pump for improved consistency and self-checks, specified vent tube areas and corresponding maximum expected pressures during cryospray procedure; optional pressure sensing capability to monitor pressure during a treatment, and improved catheter design.

Abstract: A bipolar forceps includes a shaft extending from a housing and includes an end effector assembly at its distal end. The end effector assembly has a pair of jaw members movable between an open position and a closed position. A knife assembly includes a cutter having a generally circular cross-section. The cutter is configured to cut tissue when the jaw members are in the closed position. One or more electrically conductive tissue sealing plates are disposed on each of the jaw members. The tissue sealing plates are adapted to connect to an electrosurgical energy source configured to deliver electrosurgical energy to tissue held between the jaw members to effect a tissue seal. An actuator is operably coupled to the knife assembly and is configured to selectively reciprocate the cutter relative to the jaw members.

Abstract: A surgical forceps includes a housing having a movable handle coupled thereto and movable between an initial position and a compressed position. A drive bar is operably coupled to the movable handle such that movement of the movable handle between the initial and compressed positions effects longitudinal translation of the drive bar. The drive bar further includes a coupling member disposed at a distal end thereof. An end effector assembly includes first and second jaw members movable between spaced-apart and approximated positions. Each jaw member defines a cam slot. A cam pin is slidably disposed within the cam slot of each of the jaw members. The coupling member is configured to releasably engage the cam pin such that movement of the movable handle between the initial position and the compressed position effects movement of the jaw members between the spaced-apart position and the approximated position.

Abstract: A surgical system includes a portable surgical instrument and a sleeve. The portable surgical instrument includes an end effector assembly and a housing operably coupled to the end effector assembly. The housing includes a generator and a battery assembly coupled thereto and configured to supply energy to the end effector assembly for treating tissue. The sleeve is shaped complementarily to the housing and is removably positionable about the housing. The sleeve is configured to cool the housing and/or remove heat from the housing to inhibit overheating of the generator and/or the battery assembly.

Abstract: The present invention relates to a flex-knife that enables a technique such as tissue excision to be carried out more easily, and is provided with: a rod-shaped high frequency knife which is endoscopically inserted into a body cavity and is for performing cutting procedures; a wire, the high frequency knife connected to the front end thereof; a sheath consisting of an insulating material, into which the wire is inserted; a main body, the back end of the sheath being connected thereto; and a slider to which the back end of the wire is fixed and which is disposed to the main body to enable sliding in the axial direction; wherein the high frequency knife has a large diameter part at its distal end, the large diameter part having an outer diameter that is larger than the inner diameter of the sheath.

Abstract: A catheter particularly useful for ablation lesions within a tubular region of or near the heart is provided. The catheter comprises an elongated flexible tubular catheter body having an axis and proximal and distal ends. An ablation assembly is mounted at the distal end of the tubular body. The ablation assembly has a preformed generally circular curve having an outer surface and being generally transverse to the axis of the catheter body. The ablation assembly comprises a flexible tubing having proximal and distal ends that carries a tip electrode at its distal end. An electrode lead wire extends through the catheter body and into the ablation assembly and has a distal end connected to the tip electrode. In use the distal end of the catheter is interested into the heart of a patient.

Abstract: A conduit assembly for transmitting energy between an electrosurgical energy generator and an energy delivering device comprises a first cable sub-assembly including a cable having a flexibility and an energy attenuation; a second cable sub-assembly including a cable having a flexibility and an energy attenuation; wherein the flexibility of the cable of the first cable sub-assembly is less than the flexibility of the cable of the second cable sub-assembly; and wherein the energy attenuation of the cable of the first cable sub-assembly is less than the energy attenuation of the cable of the second cable sub-assembly.

Abstract: A method of performing an ablation procedure includes the steps of inserting an antenna assembly into tissue and supplying energy thereto for application to tissue. The method also includes the step of causing contact between a first material and at least one other material disposed within the antenna assembly to thermally regulate the antenna assembly. According to another embodiment, an ablation system includes an energy delivery assembly. A first chamber is defined within the energy delivery assembly and is configured to hold a first chemical. Another chamber is defined within the energy delivery assembly and is configured to hold at least one other chemical. The first chamber and the other chamber are configured to selectively and fluidly communicate with each other to cause contact between the first chemical and the at least one other chemical to cause an endothermic reaction and/or an exothermic reaction.

Abstract: A system for generating microwave energy includes a microwave generator that generates first and second microwave signals, a transmission line and a dual antenna microwave device. The transmission line transmits the first and second microwave signals to the microwave device. The microwave device includes a first antenna proximal a second antenna and a dual-sided choke positioned therebetween. The first antenna receives the first microwave signal from the transmission line between a first conductor and a second conductor and the second antenna receives the second microwave signal between the second conductor and a third conductor. The dual-sided choke includes a first and a second antenna choke circuit. The first antenna choke circuit limits the propagation of electromagnetic fields generated by the first antenna toward the second antenna and the second antenna choke circuit limits the propagation of electromagnetic fields generated by the second antenna toward the first antenna.

Abstract: In one embodiment, a system and method for performing single-shot digital holography include an optical hybrid assembly configured to receive a reference beam from a light source and another beam, and a balanced detector comprising multiple sensor arrays that are configured to receive outputs of the optical hybrid assembly and simultaneously measure in-phase and quadrature components of an incoming light wavefront that results from interference between the reference beam and the other beam within the optical hybrid assembly to provide a full set of digital holograms in a single exposure.

Abstract: A method of treating a human eye, generally to correct vision, and preferably in one embodiment to increase the amplitude of accommodation of the lens. The method utilizes a laser to create a desired pattern within the lens. Various patterns for treating the eye lens are also disclosed.

Abstract: A counterbalancing link, a surgical system, and a method of adjusting a counterbalancing link are provided. In one embodiment, a counterbalancing link of a robotic surgical system includes a housing, and a compression spring disposed along a lengthwise axis of the housing, the compression spring having a first end and a second end. The counterbalancing link further includes a base at a first end of the housing, the base coupled to the first end of the compression spring and including at least one adjustment screw configured to adjust an orientation of the first end of the spring. A plug is disposed at a second end of the housing, the plug coupled to the second end of the compression spring and including an adjustment pin configured to adjust an orientation of the second end of the spring.

Abstract: An apparatus (650) for inserting a distal ring (9) of a wound retractor device (2) through a wound opening comprises a bladeless tip (641) for creating the wound opening by forcing tissue apart, and a conveying device (5) for conveying the distal ring (9) through the wound opening. The conveying device (5) comprises a hook element (6) for engaging the distal ring (9) to convey the distal ring (9) through the wound opening, and a receiver housing (651) for receiving a seal (652) and a proximal ring (653) of the wound retractor device (2) to hold the seal (652) and the proximal ring (653) externally of the wound opening, and thus maintain a sleeve portion of the wound retractor device (2) in tension, during conveying of the distal ring (9) through the wound opening.

Abstract: A method and apparatus providing precision external control of interventional medical procedures is presented. The apparatus includes a fixed frame, the fixed frame attachable to a patient and to a secure structure. The apparatus also includes a precision actuator in mechanical communication with the fixed frame, the actuator directing motion of a wire within a catheter or a catheter within the patient. Additionally the apparatus includes a control device in electrical communication with the actuator, wherein the control device controls the actuator.

Abstract: An obstruction detection system for a robotic catheter system including a robotic catheter manipulator assembly including one or more catheter manipulation bases and one or more sheath manipulation bases. Each manipulation base may be generally linearly movable on one or more tracks relative to the robotic catheter manipulator assembly. The obstruction detection system may include one or more obstruction detection sensors disposed on the track or on the manipulation bases to detect an obstruction along a path of motion of one or more manipulation bases. A software system may be provided for monitoring movement of the catheter and sheath manipulation bases, and/or a status of the obstruction detection sensors.

Abstract: A method of assigning an auxiliary input device to control a surgical instrument in a robotic surgical system can include automatically assigning an auxiliary input device to control an auxiliary function of a surgical instrument based on a position of the auxiliary input device and which of a user's hands is operating another input device operably coupled to control movement of the surgical instrument. A system for controlling a surgical instrument may include an input device of a surgical system that is operably coupled to generate and transmit an input control signal to control movement of a surgical instrument operably coupled to the surgical system. The system may further include an auxiliary input device, and a control system operably coupling the auxiliary input device to control an auxiliary function of the surgical instrument based on a position of the auxiliary input device and which of a user's hands is operating the input device.

Abstract: A method of determining an optimal position of a glenoid implant. The method includes identifying a center point of a patient's glenoid fossa based on an image of the patient's glenoid fossa; determining the optimal position of the glenoid implant based on the location of the center point relative to a medial point of the patient's scapula; and selecting orientation of an alignment pin based on the determined optimal glenoid implant position such that the glenoid fossa will be prepared to receive the glenoid implant at the optimal position when the glenoid fossa is prepared with a cutting device or guide coupled to the alignment pin.

Abstract: A system controller determines whether a difference of recording times of two pieces of operation log data adjacent in time sequence has a time interval equal to or longer than a predetermined time period with respect to the operation log data including identification information, operation contents for respective apparatuses that are used at a time of the surgical operation, and a recording time, and when it is determined that the difference of the recording times of the two pieces of operation log data adjacent in time sequence has a time interval equal to or longer than a predetermined time period, the system controller groups a plurality of operation log data that continue in time sequence, with a difference of the recording times of the two pieces of operation log data adjacent in time sequence being shorter than the predetermined time period, as one scene.

Abstract: Method and system for managing multiple impressions of a patient's jaw for an orthodontic treatment is provided. The method includes scanning at least a first impression and a second impression of same jaw for the orthodontic treatment; determining if the first jaw impression and the second jaw impression have distortion in different areas; selecting the first jaw impression or the second jaw impression as a base impression; and replacing a distorted tooth data from the base impression with data for the same tooth from a non-base impression. The method also includes scanning at least a first jaw impression for the orthodontic treatment; scanning a bite impression for the orthodontic treatment; matching the scanned first jaw impression with the scanned bite impression; comparing bite information with a tooth occlusal surface; and determining if reconstruction is to be performed on the tooth occlusal surface.

Abstract: An orthodontic connector assembly 10 including a plurality of substantially identical connecting members, such as members 12, 14 which include a movable but biased portion 20 which is adapted to selectively and removably receive a pocket portion 44 which is deployed on at least one bracket, such as bracket 40. In an alternative embodiment, the members, such as member 12, 14 each include a ridge, such as ridge 212, which is selectively, removably, and frictionally placed within slot 236.

Abstract: Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The goal of the pellets are to encourage sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

Abstract: A dental prosthesis component which is a member for configuring a dental prosthesis provided with an artificial tooth root, which has a high strength and a good esthetic property. The dental prosthesis component which is a member for configuring a dental prosthesis provided with an artificial tooth root wherein the dental component is made of Zr-14Nb alloy, a surface layer containing ZrO2 as a main constituent and having a thickness of 20 ?m or more and less than 80 ?m is formed on the dental prosthesis component, and the surface has a brightness of Gy 8.0 or more of the color sheets according to Practical Color Co-ordinate System 201.

Abstract: The invention relates to an angled abutment for a dental-prosthetic arrangement, in which the abutment is divided into a first sub-component and a second sub-component, wherein the first sub-component can be fixed by means of a fixing screw to an implant and has a tool opening through which a tool is able to engage to reach the screw head of the fixing screw. After the first sub-component has been fixed to an implant, the second sub-component can be connected to the first sub-component, preferably via a screwed connection, and at the same time completely covers the tool opening of the first sub-component. A retaining structure facing away from the first sub-component is formed on the second sub-component and interacts with a counter-retaining structure on a prosthesis to provide a releasable connection, which can be produced without tools, between the abutment and the prosthesis.

Abstract: A mixing tip for a dispenser according to the present invention includes a lower casing connected to the dispenser and to which a silicone base material and a curing agent are supplied, an upper casing coupled to the lower casing and including a discharge pipe through which an impression material having a desired mixing ratio of the silicone base material and the curing agent is discharged to the outside, and a mixer disposed between the lower casing and the upper casing to mix the silicone base material with the curing agent, wherein the mixer includes a mixing plate disposed between the lower casing and the upper casing and having a predetermined surface area, a shaft-fitting pipe extending downward from the mixing plate and fitted over a drive shaft of the dispenser to be rotated therewith, and a path control rib extending downward from an outer peripheral edge of the mixing plate to control flow paths of the silicone base material and the curing agent, wherein the lower casing includes a body including an

Abstract: A floss dispensing toothpaste cap having a top portion connected to a bottom portion by a hinge region. An enclosure cavity encloses a removable floss spool. A floss cutter and a floss dispenser opening pass through a side of the bottom portion. A region of the top portion reversibly covers the floss dispensing opening and floss cutter. A floss-dispensing toothpaste cap includes a bottom portion having an enclosure with a connector to connect the cap onto a toothpaste tube. A nozzle is on the bottom portion opposing the connector. A floss cutter is on a side of the bottom portion. A removable floss spool is seated over the connector within the enclosure. A top portion is connected to the bottom portion by a hinge region, and has a tab that extends over a side of the bottom cap portion covering the floss cutter in a closed position.

Abstract: A refill head, and a powered toothbrush including the same, wherein the refill head comprises a head portion including a movable tuft block that is rotated via operable coupling to a primary drive shaft of the handle. The head portion of the refill head is also receives vibrations from an eccentric that is operated by the primary drive shaft.

Abstract: The personal care appliance (10) comprises a handle/housing (20), a workpiece assembly (12), a motor assembly (18) which is mounted to the handle for driving the workpiece assembly and a secondary resonator (30) connected to the motor assembly or the handle, the secondary resonator comprising a spring mass assembly characterized in that at resonant operation thereof, vibrations produced by action of the motor assembly which would otherwise be transmitted to the handle, are significantly reduced/cancelled.

Abstract: An oral care implement that rotates about a longitudinal axis. In one aspect, the invention can be an oral care implement comprising: a head; a handle extending along a longitudinal axis and having a flat base surface; a mechanical vibratory device operatively connected to a power source, the mechanical vibratory device comprising an eccentric imparting movement to the head when activated; and wherein the flat base surface is oriented relative to the longitudinal axis of the handle so that the oral care implement can stand in a self-supporting upright orientation on a horizontal flat surface, and wherein when the oral care implement stands in the self-supporting upright orientation and the mechanical vibratory device is activated, the oral care implement rotates about the longitudinal axis while maintaining the self-supporting upright orientation.

Abstract: A totally implantable method for occluding the urethra or bladder neck utilizing an occlusive cuff connected to a control mechanism via a conduit tube. The occlusive cuff is reversibly changed from an activated (occlusive condition) to a de-activated (non-occlusive) condition by depressing a deactivation button contained within a resilient, elastomeric sheath surrounding the control mechanism. The occlusive condition is once again obtained by depressing an activation button also situated within the resilient sheath. In the occlusive condition, a preset tension is applied to a flexible diaphragm through a tensioning suture by a constant force spring contained within the control mechanism. This tension is translated into an occlusive pressure applied to the urethra or bladder neck sufficient to prevent urinary leakage.

Abstract: In one embodiment, an implant includes a body member and an extension member. The body member is formed of a first material and has a first side portion and a second side portion. The extension member is formed of a second material different than the first material. The extension member has a first arm portion, a second arm portion, and a mid-portion disposed between the first arm portion and the second arm portion. The mid-portion extends from the first side portion of the body member to the second side portion of the body member. The first arm portion extends from the first side portion of the body member along a first axis. The second arm portion extends from the second side portion of the body member along a second axis different than the first axis.

Abstract: A system for closing an aperture in a biological tissue includes an implant deployment device having a frame arm, a clip connected to the frame arm, and a lock bar including a protrusion. The protrusion extends away from the frame arm and is configured for selectively holding the clip in an open position or a closed position. A surgical implant is releasably attached to the frame arm. The clip retains the surgical implant in contact with the frame arm when the clip is in the closed position and the clip allows the surgical implant to be separated from the frame arm when the clip is in the open position.

Abstract: A parent artery occlusion (PAO) device which provides for immediate occlusion of a cerebral artery to isolate a defect. The PAO device includes a self-expanding wire-frame prolate structure which is partially covered with an ePTFE membrane.

Abstract: A device for retrieving items endovascularly includes a sheath having a first lumen containing a snare that can be deployed out a distal end of the sheath and retracted back into the sheath for pulling an IVC filter into the sheath. The sheath has a second lumen that opens through a sidewall of the sheath proximal of the distal end. The second lumen contains a removal assist device that can be deployed through the sidewall and used to dislodge and/or cut an item to be retrieved from a vein wall. The removal assist device includes a catheter, a cutting head, and a pull wire. The pull wire has a proximal portion protruding from a proximal end of the catheter and a distal end connected to the cutting head. The pull wire is movable within the catheter to selectively extend and retract the cutting head from the distal end of the catheter.

Abstract: Embolic protection aspirators and methods for extracting debris from the vasculature during interventional procedures are provided. One such system may include an aspirating filter delivery catheter having a filtration device, an operable end cap, and a plurality of aspiration ports. The delivery catheter may be fluidly coupled to a suction providing means for extracting debris while traversing a target site for distal delivery of the filtration device. Another such system may include an aspirating filter retrieval catheter having an aspiration lumen and a balloon. The aspiration lumen may be fluidly coupled to a suction providing means for extracting debris from the filtration device prior to and/or during retrieval of the filtration device. By inflating the balloon to partially or fully restrict blood flow, suction pressure proximal of the filtration device may be increased to enhance debris extraction.