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1532 results about "Inner/Lumen Diameter" patented technology
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Circular stapler buttress
A buttress for use with circular surgical staplers that does not require adhesive to securely fasten the buttress to the stapler. Following cutting and stapling by the circular stapler, the buttress has an adaptive opening through its central region with a diameter smaller than the outer diameter of the stapler anvil. Because of relief features built into the buttress, the stapler anvil may be pulled through the buttress material without causing permanent alteration to the buttress. These relief features may be provided regardless of whether the buttress is made of inelastic or elastic materials. The buttress is generally circular in shape with an outer diameter sized to coincide with the outer diameter of the stapler body staple compression surface and the outer diameter of the anvil compression surface of a circular stapler with which it is used. Prior to surgical use, the buttress is attached to the stapler with disruptable portions extending from outer perimetal areas of the buttress.
Owner:WL GORE & ASSOC INC
Easily placeable and removable wound retractor
InactiveUS20060149137A1Easy to placeGood for scrollingCannulasSurgical needlesSurgical departmentBody tissue
The invention is directed to a surgical wound retractor for retracting and sealing an incision and forming a functional opening or channel through which a surgical procedure may be executed. The wound retractor provides a path for a surgeon to insert his hand and / or instruments through the opening formed by the wound retractor. The wound retractor is sized and configured to be easily placed through a small incision and removed without further insult to the body tissue adjacent to the incision. The wound retractor is adapted to dilate a surgical wound incision to a desired diameter, and comprises a first ring having a diameter greater than the desired diameter of the wound incision and being adapted for disposition interiorly of the wound incision; a second ring having an annular axis and a diameter greater than the desired diameter of the wound incision and being adapted for disposition exteriorly of the wound incision; and a flexible sleeve disposed in a generally cylindrical form between the first ring and the second ring, the first ring having at least one notch to facilitate folding or collapsing of the first ring during insertion and removal of the first ring through the wound incision. The first ring may further comprise a second notch disposed on an opposing end of the first notch to further facilitate folding or collapsing of the first ring. With this aspect, the first ring is folded by squeezing between the first and second notches during insertion and removal of the retractor from the incision. In another aspect, the wound retractor may further comprise a tether having a length, a first end attached to the first ring interiorly of the sheath, and a second end disposed outside of the wound incision, wherein the tether facilitates removal of the first ring by pulling on the second end to retrieve the first ring through the wound incision.
Owner:APPL MEDICAL RESOURCES CORP
Systems And Methods For Removing Obstructive Matter From Body Lumens And Treating Vascular Defects
InactiveUS20120101510A1Increase blood flowHigh trafficMulti-lumen catheterCannulasMedicineDistal portion
Systems and methods for removing obstructions from, delivering implantable devices or substances in or near and / or restoring flow through body lumens, such as blood vessel lumens. A catheter having a proximal portion of a first diameter and a distal portion of a second diameter (smaller than the first diameter) is advanced into a body lumen. The distal portion of the catheter is caused to expand to a diameter that is larger than the second diameter but no larger than the first diameter. A working device is then advanced out of the distal end of the catheter and used to remove obstructive matter, deliver an implantable device or substance and / or restore flow. The distal portion can be reduced in diameter prior to removal from the body.
Owner:TYCO HEALTHCARE GRP LP
Systems and methods for compartmental replacement in a knee
A knee replacement system provides a knee implant that may be used to more accurately replicate the diameter of a natural knee. In one embodiment, a patellofemoral component is connected to the posterior portion of a condylar component by screws that pass through the femur allowing the patellofemoral component and the condylar component to be torqued against opposing sides of the femur. Two additional screws are used to connect the patellofemoral component to an anterior portion of the condylar component. A gap may be left between the patellofemoral component and the anterior portion of the condylar component if needed to provide precise replication of the diameter of the natural knee from the patellofemoral component to the condylar component.
Owner:DEPUY PROD INC
Posterior lumbar intervertebral stabilizer
A posterior intervertebral stabilizer includes: a first stabilizing element having: (i) a first surface operable to engage an endplate of a first vertebral bone of a spine, and (ii) a second surface spaced apart from the first surface and operable to engage an endplate of an adjacent second vertebral bone of the spine; a second stabilizing element having: (i) a first surface operable to engage an endplate of the first vertebral bone of the spine, and (ii) a second surface spaced apart from the first surface and operable to engage an endplate of the adjacent second vertebral bone of the spine; and respective spring elements, each including helical coils, disposed between the respective first and second surfaces of the first and second stabilizing elements, each operable to provide a reactive force in response to compression loads from the first and second vertebral bones, wherein at least some diameters of respective turns of the respective helical coils differ.
Owner:CARDO MEDICAL
Braided occlusion device having repeating expanded volume segments separated by articulation segments
InactiveUS8361138B2Occlude a vessel, channel, lumen, or cavity quicklyMeet high volumeDilatorsOcculdersBody organsMedical device
The present invention provides a flexible, low profile vascular occlusion device having large volume filling capability and high metal content for fast occlusion, of the type fabricated from braided tubular metal fabric having an expanded preset configuration and an elongated collapsed reduced diameter configuration for delivery through a catheter to a treatment site and shaped to create an occlusion of an abnormal opening in a body organ or vessel, the woven metal fabric having a memory property whereby the medical device tends to return to said expanded preset configuration when unconstrained. The device further includes a first shape formed from the braided tubular fabric consisting of a repeating pattern of expanded volume segments separated by small diameter articulation segments and a second overall device shape comprised of the first shape formed about itself in various shapes to occlude a vessel. In one embodiment a shaping wire contained coaxially within the tubular braid, provides or assists in the formation of the second overall device shape.
Owner:ST JUDE MEDICAL CARDILOGY DIV INC
Method and apparatus for providing a relative location indication during a surgical procedure
An orthopedic guidewire includes an elongate guidewire body having longitudinally spaced proximal and distal guidewire ends. An engaging feature is located at the distal guidewire end and is configured to selectively engage a bone surface. At least one of a variable diameter and a variable stiffness are along a portion of the guidewire body spaced apart from the engaging feature. A method of providing a relative location indication during a surgical procedure utilizing the orthopedic guidewire is also included.
Owner:THE CLEVELAND CLINIC FOUND
Implantable and lumen-supporting stents and related methods of manufacture and use
InactiveUS20090105809A1Improve expansion propertiesImprove featuresStentsBlood vesselsVisibilityLateral bending
An implantable stent includes multiple circumferential segments that surround a bore and are connected in series along a length to form a tubular wall. Multiple adjacent alternating opposite facing crowns arranged along each segment's circumference are bridged by struts. The struts include a series of staggered arcuate edges with limited flats to provide a limited region of maximum width between significantly extended reducing diameter tapers at either end where they transition into the crowns. Connections between adjacent segments are wider and stiffer than the struts and strut-crown transitions in the segments. The crowns include inner and outer radii with off-set centers along a common axis to provide medial crown peaks along the axis that are wider than the narrowed crown shoulders on either side of the axis and from which the tapered struts extend. Material strain and flexure along the stent during lateral bending is distributed mainly within the segments, e.g. along the struts or crowns, versus at the connections between segments. Material strain and deformation during radial expansion is principally concentrated at the crown shoulders and tapered transition region with the struts. Particular closed-open-closed arrangements along the stent length are disclosed, though with fewer stent connections in the relatively “closed” end-portions along the stent than are provided by other typically “open” cell stents in prior use. Enhanced combinations of performance characteristics are provided regarding visibility, trackability, expansion characteristics, fatigue failures, coating integrity, and local drug delivery from the stent.
Owner:MEDLOGICS DEVICE CORP
Apparatus and methods for treating bone
ActiveUS20070055274A1Increased radialIncreasing diameter of coilInternal osteosythesisSpinal implantsFiberBobbin
Implants and methods for bone treatment, preferably minimally invasive treatment, including repositioning of vertebrae may comprise insertion of a bobbin having a wire, string, thread or band, coiled around the bobbin. During coiling, the diameter of the bobbing/band complex may increase. Such increase in diameter can push against the inner side of the endplates of the vertebral body, and augment the vertebral body to its original height. The implant may also take the form of a coiled sleeve which when inserted into the vertebral body is uncoiled. The force of the uncoiling sleeve pushes against the inner side o the endplates of the vertebral body, restoring the vertebral body to its original height. The implant may also take the form of fibrous masses comprised of a thread or other relatively thin structure, for example a fiber or strand, of any biocompatible material having desired characteristics, for example a shape memory alloy, titanium, stainless steel, another metal or metal alloy, a ceramic, a composite or any combination thereof. The, strand, thread or other fiber may be coiled, woven, matted, tangled or otherwise formed into a wool-like mass or body having a desired configuration. Expansion of the expandable member within the vertebral body or other bone may reposition the fractured bone to a desired height and augment the bone to maintain the desired height. A bone cement or other filler can be added to further treat and stabilize the vertebral body or other bone.
Owner:SYNTHES USA
Valve assembly including diameter reduction structure for trocar
InactiveUS7025747B2Convenient introductionSmall sizeCannulasInfusion syringes% diameter reductionVALVE PORT
A valve assembly and diameter reduction structure for trocar employing a movable diameter reduction structure. The diameter reduction structure is positioned in proximity to a first seal and includes a plurality of stand off members movable between a first position, a second position, and a third position. The diameter reduction structure in the first position reduces the likelihood of the first seal losing its integrity by limiting excessive off-axis and angular movements of small diameter surgical instruments. When large diameter surgical instruments are positioned through the trocar, the diameter reduction structure pivots to accommodate the passage of larger diameter surgical instruments without any operational adjustments.
Owner:TYCO HEALTHCARE GRP LP
Magnetic devices and applications for medical/surgical procedures and methods for using same
InactiveUS20070142780A1Facilitate manipulationEasy alignmentCannulasInfusion syringesEngineeringReducer
One embodiment of the invention comprises a trocar and a reducer cap that magnetically attaches to the trocar. The trocar and the cap each include a magnetic member, at least one of which is a first magnet, and the other of which is either a second magnet or a non-magnetized magnetically permeable member. Including a magnet of sufficient strength in the trocar and/or the cap will create a magnetic field that automatically holds a surgical instrument having a magnetically permeable member at its tip in axial alignment with the cap or trocar lumen. Introduction of the surgical instrument into the lumen can be further facilitated by providing the trocar or cap lumen with a funnel-shaped opening. A lumen seal can be provided by one or more compliant toroidal seal members that expand radially inwardly when compressed axially by the magnetic attraction between the cap and trocar. The alignment feature is particularly advantageous when incorporated in a mini-trocar having a lumen on the order of 1-3 mm in diameter. In that case, a trocar cap can be a small disc magnetically attracted to the trocar to cover the lumen. Magnetic aligning devices according to the invention can be used internally of a patient or transdermally. Another embodiment of the invention is an ostium plug with a lumen therethrough that can be used in tubal sterilization. The plug is permanently implanted in the patient, but a cap is coupled magnetically to the proximal end of the plug to permit reopening of the lumen when desired.
Owner:VAN LUE VETERINARY SURGICAL
Internal compression tourniquet catheter system and method for wound track navigation and hemorrhage control
An internal compression tourniquet catheter system and method for controlling hemorrhage from wounds, particularly penetrating wounds. Its construction includes an inflatable member constructed of very thin, flexible, biocompatible, and nonelastic and puncture resistant material such that when deflated it lies flat and can be wrapped around the catheter shaft, which passes within and has a lumen to inflate it, to minimize overall diameter when deflated for insertion into the tissue track created by the wounding agent. The inflatable member is of large potential volume enabling full inflation with near zero internal pressure when unconstrained externally. When positioned within a wound track and inflated, the gas or liquid injected into the balloon lumen creates pressure because its expansion is constrained by the tissues of the wound, and that pressure is transmitted directly to the surrounding tissue of the wound track. The pressure exerted on the tissue can be precisely measured and controlled, automatically if appropriate, such that sufficient pressure is applied to tamponade bleeding, but not damage tissue. Since the balloon is of large potential volume, it can easily expand to fill and compress small, large, and irregular wound tracks and can successfully tamponade wounds that smaller, elastic balloon catheters would be unable to tamponade. The catheter system includes means to assist insertion into the wound track, including a rounded or bulbous exploring tip and an internal stylet with an external orientable handle. The distal end of the catheter-stylet assembly can be bent slightly to allow following a curved or irregular wound track, such wound track navigation further assisted by twisting the stylet handle to orient the bent catheter tip within the wound track.
Owner:CARDIOCOMMAND
Expanded UHMWPE for guiding catheter liners and other lubricious coatings
An intraluminal catheter, such as a guiding catheter, employed for intravascular procedures and having an inner liner formed of expanded Ultra High Molecular Weight Polyethylene (UHMWPE) is disclosed. The expanded UHMWPE is microporous and has an oriented microstructure structure characterized by nodes interconnected by fibrils. The inner liner formed of expanded UHMWPE is very thin to maximize the inner lumen diameter and has excellent mechanical properties.
Owner:ABBOTT CARDIOVASCULAR
Centering catheter
A catheter with at least one centering device attached near a distal end of the catheter. The centering device has at least two struts extending between a proximal end and a distal end. The centering device has a variable diameter and tends to center the distal end of the catheter, steering the catheter away from the vessel wall during insertion through the vasculature and toward the treatment site. The centering catheter may facilitate access to tortuous anatomy by preventing the catheter tip from catching on irregularities in the lumenal surface. The centering catheter may also facilitate uniform stent expansion by stabilizing the catheter during stent deployment.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH
Trocar seal
InactiveUS20050209608A1Increase the diameterUniform diameterEar treatmentCannulasSurgical deviceGeneral surgery
A seal is disclosed for installation on the proximal end of a trocar to seal on surgical instruments having varying diameters. The seal has a general hourglass shape with an upper portion, a bottom portion and a sealing portion interposed between the upper and bottom portions. The bottom portion is formed for mating engagement with the access port at the proximal end of the trocar. A passage exists between the upper and bottom portions, and the diameter is expandable from 2 mm to about 13 mm. Various configurations of such a seal are disclosed.
Owner:COOPERSURGICAL INC
Expandable cerebrovascular sheath and method of use
Disclosed is an expandable transluminal sheath, for introduction into the body while in a first, small cross-sectional area configuration, and subsequent expansion of at least a part of the distal end of the sheath to a second, enlarged cross-sectional configuration. The sheath is configured for use in the upper vascular system and has utility in the introduction and removal of therapeutic or diagnostic microcatheters. The access route is through the femoral arteries or the iliac arteries to the cerebrovasculature. The distal end of the sheath is maintained in the first, low cross-sectional configuration during advancement to the cerebrovasculature. The distal end of the sheath is subsequently expanded using a radial dilatation device, which is removed prior to the introduction of microcatheters. The sheath can be inserted in a first, small cross-sectional configuration, be expanded diametrically to a second, larger cross-sectional configuration, and then be reduced to a diametrically smaller size for removal.
Owner:ONSET MEDICAL CORP
Adjustable bone stabilizing frame system
InactiveUS6613049B2Easy and fast assemblyEasy constructionInvalid friendly devicesFractureEngineeringIliac screw
By providing components securable to anchor pins or screws of different diameters as well as providing clamps which hold associated pins in any position during adjustments, an external fixation or adjustable frame structure is provided which is capable of being quickly and easily assembled in any desired configuration. In the present invention, the frame structure is retained in any assembled configuration in order to allow final adjustments to be made, prior to the final securement of the frame assembly in the precisely desired configuration by closure of each clamp member. In this way, an entire frame assembly is capable of being constructed, adjusted, and readjusted in order to assure each component is oriented in the precisely desired position prior to final closure of the clamping members. In one preferred embodiment, the clamping members employed in the frame structure of the present invention incorporate friction pins internally mounted in each clamp which engages the rod member once this rod is inserted into the jaws of the clamp. In this way, any rod member inserted into the clamping jaws contacts the surface of the jaws and the friction pin, preventing the rod member from sliding or moving relative to the clamp. In addition, by incorporating a uniquely constructed, moving wedge plate that is adjustably engageable with any cooperating anchor pin, secure affixation of the mounting member with the anchor pins of any diameter is easily achieved, regardless of the orientation configuration, or diameter of the anchor pin.
Owner:ZIMMER INC
Expandable intraluminal endoprosthesis
An expandable intraluminal endoprosthesis including a tubular member (1) a first diameter which permits intraluminal delivery of the member into a lumen of a body passageway, particularly a blood vessel. The tubular member (1) is capable of acquiring a second, expanded and deformed diameter upon the application from the interior of the tubular member of a radially outwardly extending force, which second diameter is variable and dependent on the amount of the force applied to the tubular member. Such a tubular member may be expanded and deformed to expand the lumen of the body passageway. The wall of the tubular member includes a substantially continuous structure (2) of mutually staggered undulations. This structure has been separated from a tube wall and exhibits at least one pattern which advances substantially helically along a longitudinal axis of the tubular member. Connection elements within the structure connect adjacent undulations to each other. These connection elements are an integral extension of the undulations thereby interconnected.
Owner:ORBUSNEICH MEDICAL PTE LTD
Occlusion Device
ActiveUS20150313605A1Minimization requirementsReduce riskDilatorsDiagnostic markersMedicineBlood vessel
Provided herein is an occlusion device for intrasaccular implantation and/or vascular occlusion comprising: (a) a substantially solid marker having a proximal end, and a distal end; and (b) a low profile resilient mesh body attached to the distal end of the marker, the body having a delivery shape and a deployed shape capable of conforming to aneurysm walls; wherein the body has a diameter greater than a diameter of an aneurysm to be treated. Also provided herein is a kit comprising the occlusion device disclosed herein and a means for delivery thereof. Methods of manufacture and use of the occlusion device disclosed herein are also disclosed.
Owner:CERUS ENDOVASCULAR
Method for securing a glenoid component to a scapula
A medical procedure includes providing a prosthesis which includes (i) a body portion having a rear surface and a bearing surface, and (ii) an anchor peg including a shaft extending from the rear surface of the body portion, wherein the anchor peg includes a plurality of outwardly extending fins secured to the shaft, and further wherein the plurality of outwardly extending fins each possesses a first diameter. The medical procedure further includes creating an anchor hole in a natural bone, the anchor hole possessing a second diameter which is less than the first diameter. In addition, the method procedure includes positioning the anchor peg within the anchor hole so that each of the plurality of outwardly extending fins deforms so as to possess (i) a concave side which faces an open end of the anchor hole, and (ii) a convex side that faces a closed end of the anchor hole.
Owner:DEPUY PROD INC
Expandable sheath introducer
The disclosure relates to an a catheter sheath introducer that is capable of being expanded from first diameter to second diameter in order to accommodate differently sized medical devices to be introduced by the sheath introducer. The device is structured such that it does not foreshorten when expanded.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH
Method and apparatus for treating varicose veins
Apparatus for occluding a blood vessel, the apparatus comprising:
an occluder, the occluder being configured so that at least a portion of the occluder may assume (i) a diametrically-reduced configuration for disposition within the lumen of a tube, and (ii) a diametrically-expanded configuration for disposition adjacent to the blood vessel, such that when said at least a portion of the occluder is in its diametrically-expanded configuration adjacent to the blood vessel, the occluder will cause occlusion of the blood vessel.
Owner:AMSEL MEDICAL CORP
Polymer-based stent assembly
Methods for preparing a polymer-based stent assembly comprising an inflatable balloon catheter and a polymer-based stent resistant to relaxation-related negative recoil are provided. The methods comprise heating a polymeric cylindrical device which is at a final predetermined shape and diameter to a temperature sufficiently above the glass transition temperature (Tg) of the polymer and for a time sufficient to erase any memory of previous processing of the polymeric cylindrical device and then quenching the polymeric cylindrical device to provide an educated polymeric cylindrical device having a memory of the final predetermined diameter and shape, mounting the educated cylindrical device on an inflatable balloon catheter, reducing the diameter of the educated cylindrical device by heating to a temperature at or slightly above the Tg of the polymer while evenly applying pressure on the exterior surface of the wall of the cylindrical device, and then cooling the cylindrical device below the Tg of the polymer to provide a stent assembly comprising an inflatable balloon catheter and an expandable, educated, polymeric stent snugly and stably disposed thereon. Assemblies comprising an inflatable balloon and a polymer based stent that is substantially resistant to relaxation related recoil mounted snugly on the balloon are also provided.Owner:SAHAJANAND TECHNOLOGIES PRIVATE LTD
Surgical thread and cosmetic surgery method
A surgical thread is made of a metal, polymer or biological material embodied in the form of a spiral whose diameter ranges from 0.5 to 5 mm. The thread has a diameter ranging from 0.1 to 1 mm and exhibits the properties of a compression or extension spring obtainable by heat treatment. Also a method is disclosed which is characterized in that it consists in introducing the spiral-shaped thread into subcutaneous soft tissues in order to tighten and fix said tissues by means of a puncture needle in bore of which a thread-spiral exhibiting the properties of a compression or extension spring is fixed from outside or from inside. When the needle is extracted the thread-spiral remains under skin preserving the compression or extension properties thereof, thereby producing a skin compression or extension effect.
Owner:SULAMANIDZE MARLEN ANDREEVICH +1
Mandibular advancement device, and a method and kit for preparing said device
InactiveUS20150216716A1Effective treatmentImprove comfortOthrodonticsSnoring preventionEngineeringLateral protrusion
Mandibular advancement device (1; 20) and a device preparation method and kit, comprising a mouthpiece (2) and at least one plastic strap (5; 21) with two ends (7) fitted with a slot (9) that is connected articulately to a respective cylindrical portion (11) of a lateral protrusion (10) of the mouthpiece (2). The slot (9) is closed and is longer in length than the diameter of the cylindrical portion (11), which can move along the slot (9). The strap (5; 21) acts by traction between the cylindrical portions (11) of the mouthpiece (2) to prevent the free return of the lower portion (4) with respect to the upper portion (3) of the mouthpiece (2) and therefore treats apnea, whilst allowing some advancement and lateral movement of the lower portion (4), making it comfortable for the user.
Owner:BIOTECHNOLOGY INST I MAS D SL
Polyaxial bonescrew assembly
A bone screw assembly includes a screw, an outer housing, and an inner housing. The screw includes a shank and a head. The outer housing has a proximal end, a distal end, and a passageway extending longitudinally therethrough. The outer housing defines a saddle at the proximal end thereof for receiving at least a portion of a rod therein. The inner housing is positionable within the passageway of the outer housing. The inner housing has a recessed distal portion for receiving the head of the screw therein. The inner housing also includes a proximal surface defining a substantially V-shaped configuration for receiving rods of different diameters therein.
Owner:K2M
Balloon Catheter
InactiveUS20070255207A1Easy to manufactureSimple structureStentsBalloon catheterBalloon catheterBiomedical engineering
A balloon catheter for medical treatments easily manufacturable at low cost by a rather simple structure by providing a smaller diameter non-profile balloon catheter by eliminating the need for adhesion and welding of a balloon and eliminating extra profile at a connection part between the balloon and a shaft, wherein PTFE may be used for the shaft, and silicone may be used for the balloon. A inside hollow shaft (3) formed of a balloon material is inserted into an outside hollow shaft (2) formed of a shaft material, and the tip part of the inside hollow shaft (3) is projected from the tip end of the outside hollow shaft (2) to manufacture a double-tube catheter shaft (2). An expandable balloon (5) is formed of the projected portion of the inside hollow shaft (3), a cap (4) is fitted to the tip of the inside hollow shaft (3), and the PTFE is used for the outside hollow shaft (2), with the silicone used for the inside hollow shaft (3).
Owner:HANGAI MASANORI +1
Cement/biologics inserter and method for bone-fastener fixation augmentation
An inserter and associated method improve the placement of a fastener into a bone. Although ideally suited to the placement of a pedicle screw into a vertebral body (VB), the apparatus and method are applicable to other bones and fasteners, pins, and the like. The apparatus includes cannulated body having a proximal end, a distal end, and a threaded section therebetween. The proximal end is shaped for rotational tightening by a wrench or other tool, and the distal end including a perforated nozzle so that cement and / or biologics may be injected into the bone through the cannulated body. The proximal end includes a Lur-loc or other appropriate fitting to receive a cement-filled syringe. The device is also preferably disposable using, for example, clear plastic construction. The inserter may further including a member for sealing the nozzle relative to a bone. Such a member may be composed of a silatstic or other compressible material, or may be inflatable. At least the distal end of the device is preferably provided with varying diameters for different insertion sizes.
Owner:SINTEA PLUSTEK
Tube connection assembly
InactiveUS7393019B2Simple structurePrevent rotationPipe elementsCouplingsAnatomyBiomedical engineering
A tube connection assembly comprises a male member, a female member and a mating member. The male member is provided with a retaining part that is formed with a non-circular cross-section on the outer peripheral part of a male body. The mating member is held by the retaining part, is formed from an elastic material having a C-shape, and has, on a portion thereof, mating parts. The female member is provided with a receiving part in which the male member is inserted, and mating holes and formed through the receiving part. The mating member is held, so as to prevent rotation, by a base part of a retaining part that has a non-circular cross-section as a part of the outer peripheral part of the male body, and decreases or increases in diameter in the radial direction to mate with the female member through insertion into the mating holes.
Owner:TOYODA GOSEI CO LTD
Ostial stent
InactiveUS20050177221A1Less subject to movementLess to other complicationStentsBlood vesselsBiomedical engineeringBlood vessel
The specification discloses a cardiovascular ostial stents, a ostial stent balloon, and methods for their use. The stent includes two portions having different degrees of expandability. The distal portion has a normal degree of expandability to support a vessel. The proximal portion has a higher degree of expandability so that it can be formed into a flange-like structure. The balloon is designed to deploy the new stent in a single operation. The balloon includes first and proximal portions having different diameters corresponding to the first and proximal portions of the stent. The distal portion is of normal diameter to deploy the distal portion of the stent in the vessel. The proximal portion is of greater diameter to form the proximal portion of the stent into the flange-like structure. The method involves deploying a conventional stent through one branch of the bifurcation, and then deploying one of the novel stent through a wall of the first stent and into the other branch. The flange-like structure on the novel stent secures the novel stent within the conventional stent. Finally, a one-piece Y-shaped stent is provided for placement in a bifurcated artery.
Owner:SQUAREONE
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