Abstract: A detachable balloon system includes an inflatable balloon with a self-sealing valve. The balloon has an elastomeric membrane and a proximal opening. The self-sealing valve is made up of a valve body for receiving an inflation instrument to inflate the balloon. The valve body is preferably formed of a biocompatible elastomeric material and includes a base portion and a sealing portion. The base portion is bonded to the elastomeric membrane so as to seal the proximal opening of the balloon. The sealing portion is located within the balloon and extends distally from the base into the balloon. The sealing portion is compressibly sealable in response to a pressure within the balloon following inflation of the balloon and removal of the inflation instrument. A balloon dispenser for housing a balloon prior to receipt of an inflation instrument is also described.

Abstract: The occlusion balloon catheter includes an elongated tubular catheter body having a fluid lumen for inflation of an occlusion balloon detachably mounted to the catheter body by a tubular shape memory collar. The occlusion balloon includes a valve for sealing the occlusion balloon when it is inflated, and the collar of shape memory material clamps onto a stem of the valve. The shape memory collar can be heated by a fiber optic pusher member threaded through the catheter body to cause the collar to assume an enlarged configuration disconnecting the occlusion balloon. A method of detaching the occlusion balloon from the occlusion balloon catheter involves the steps of placing the occlusion balloon catheter within a guiding catheter, and placing the guiding catheter within the vasculature so that the distal opening of the guiding catheter extends into an aneurysm or other deformation to be treated. The fiber optic pusher is then used to expel the device into the aneurysm.

Abstract: A self-expanding filtration element is fitted to the distal end of a catheter while a sheath for constraining such element to a reduced diameter is mechanically manipulatable from the proximal end of the device. The entire device is maneuvered into position over a guide wire and deployed prior to treatment of the body lumen at an upstream location. After completion of the treatment procedure, the filtration element is collapsed and constrained within the sheath to retain any embolic material that has been captured and allow it to be safely removed from the vasculature. The device may be combined with a primary treatment modality and its low profile allows the constrained filtration element to be removed through a deployed stent.

Abstract: An aortoiliac intraluminal grafting system incorporating novel structural features for enhancing the effective and efficient deployment of a tapered prosthesis having at least one attachment system, in the vessel of an animal body, the system including a balloon catheter assembly, an inferior capsule catheter assembly, a superior capsule assembly and means interacting therewith, and a capsule jacket assembly. The capsule assemblies include an inferior capsule and a superior capsule, wherein the attachment systems of the tapered prosthesis are disposed within the two capsules. The tapered prosthesis embodies a main tubular member and an inferior tubular portion, having attachment systems secured to the superior end of the main tubular member and the inferior end of the inferior tubular portion. An occlusive device and deployment catheter is also disclosed.

Abstract: An intravascular catheter system for properly implanting a stent in a body lumen generally comprising a catheter having an elongated shaft with an inflatable balloon formed of compliant material and a stent mounted on the working length of the balloon. The balloon material is compliant within the working range of the balloon to provide substantial radial expansion. The wingless radially expansive balloon expands in a uniform manner, thereby producing uniform expansion and implantation of the stent.

Abstract: A dilating and support apparatus with disease inhibitors and methods for use is disclosed that is particularly useful for repairing and/or serving as a conduit for body passageways that require reinforcement, dilatation, disease prevention or the like. Such apparatuses are utilized to deliver a therapy, that therapy being from a family of devices, drugs, or any of a variety of other elements to a specific location within the body. The instant disclosure provides a system of combining a novel radial deployment and/or drug delivery therapy with existing balloon dilatation therapy into one device. This combination will yield a significant decrease in cost to the healthcare system as well as providing a therapy to the patient with increased safety and efficacy. Further, the instant invention provides a novel and improved platform for synthetic/tissue interface between the device and the body.

Abstract: A body tissue graft for use in a patient includes a frame structure made of a first elastic material, a covering of a second elastic material on the frame structure, the covering substantially filling openings in the frame structure, and a connector connected to the frame structure. Projections are secured to the connector structure. The projections facilitate attachment of the tubular graft in a patient by securing the graft to the body tissue with which the graft is employed. The connector selectively circumferentially expands and the projections selectively circumferentially expand. This may be done using an inflatable balloon to circumferentially expand the projections. A restraining member may be provided to restrain the projections in a cone shape so that an end of the graft may be used to open an aperture through a side wall of existing body organ tubing and a portion of the projections may enter the aperture.

Abstract: Shape memory alloy and elastically self-expanding endoluminal support structures which are at least partially encapsulated in a substantially monolithic expanded polytetrafluoroethylene (“ePTFE”) covering. An endoluminal stent, which has a reduced diametric dimension for endoluminal delivery and a larger in vivo final diametric diameter, is encapsulated in an ePTFE covering which circumferentially covers both the luminal and abluminal walls along at least a portion of the longitudinal extent of the endoluminal stent. The stent and ePTFE covering are helically wound into an open cylindrical configuration with adjacent windings forming overlapping regions of ePTFE covering bonded to one another.

Abstract: A jacketed stent assembly comprising a tubular, expandable stent, preferably having a metallic framework, jacketed with a cylinder of biocompatible, non-thrombogenic expandable material, such as heterologous tissue, which, in a preferred embodiment, contains a therapeutic or diagnostic agent. In a preferred embodiment, the jacket of the expandable stent is formed of bovine or porcine pericardial tissue. A delivery catheter having an expandable member on its distal extremity may be used to deliver the stent assembly to a desired region in a lumen of a patient. The jacketed stent is expanded to be seated within the body lumen.

Abstract: The present invention provides an improved stent delivery catheter. The stent delivery system comprises a catheter with a retractable sheath arranged concentrically near its distal end. The retractable sheath is connected to a pull wire for retraction. A sliding seal connects the proximal end of the retractable sheath and the catheter. This seal forms a fluid tight chamber when the retractable sheath is in the unretracted position, allowing the delivery system to be prepared by filling the fluid tight chamber with fluid to flush out air prior to insertion into the vasculature of the patient.

Abstract: A delivery catheter for a radially expandable intraluminal stent or stented graft. The delivery catheter comprises an elongate catheter body defining proximal and distal ends and at least one lumen extending longitudinally therethrough. Disposed on the catheter body at a location proximal to the distal end thereof is an inflatable, expandable balloon. The balloon is at least partially fabricated from a conformable material for allowing the stent to be at least partially embedded therein when positioned thereupon.

Abstract: A stent of high longitudinal flexibility includes multiple ring elements coupled together to be articulating without fixed physical attachment therebetween when the stent is in an unexpanded state, and to uncouple automatically while maintaining their positional relationship when the stent is deployed to an expanded state. The stent is fabricated to offer radial strength suitable for supporting a wall of a vessel, duct or tract of a patient in which the stent is to be implanted, against recoil of the wall in response to deployment of the stent. The fabrication process includes forming a plurality of common ring elements aligned along a longitudinal axis; and fashioning coupling elements on each of the ring elements to mate with and pivot longitudinally relative to coupling elements fashioned on neighboring ring elements without fixed physical attachment between the coupling elements.

Abstract: Catheters including a rugged, reusable proximal body and a disposable distal body attached by a releasable connection are provided. The reusable proximal body is constructed from resterilizable materials such as glass, metal alloys and engineering plastics. The disposable distal body, designed for one-time use, is made from reliable but inexpensive materials. The catheters may be dilatation catheters and may be manufactured in any configuration, including rapid exchange, balloon-on-a-wire, and over-the-wire designs with single or multiple lumens. The modular construction of the catheter and releasable connection provides for rapid and easy changes in the configuration and balloon size depending on the needs of the medical procedure.

Abstract: A stent having marker tabs formed from a micro-alloyed combination of materials provides for more precise placement and post-procedural visualization in a vessel, by increasing the radiopacity of the stent under X-ray fluoroscopy. A unique micro-alloying process is utilized to form the tabs, comprising a first alloy and a second alloy, wherein one of these alloys is radiopaque. This substantially eliminates the possibility of galvanic action between the tab and the stent. This process is also applicable to other medical devices.

Abstract: A stent deployment catheter includes a catheter body extending to an elongated distal end portion adapted for supporting and deploying a stent having a cylindrically shaped sidewall expandable in a vessel lumen to treat lesions. The distal end portion bearing the stent is guided within vessel lumen to a site therein to treat the lesions. Two guide wires are placed one in each of the bifurcations of a branched vessel. A guide wire lumen in the catheter is used to direct the elongated distal end portion along the guide wire to a vessel branch containing the lesions and a side branch guide wire lumen protectively isolates a length of a side branch guide wire from the stent when supported by the elongated distal end portion to establish a predetermined deployment site for a distal end portion and a proximal end portion of the stent for treating lesions of the first branch.

Abstract: A coating composition for use in coating implantable medical devices to improve their ability to release bioactive agents in vivo. The coating composition is particularly adapted for use with devices that undergo significant flexion and/or expansion in the course of their delivery and/or use, such as stents and catheters. The composition includes the bioactive agent in combination with a mixture of a first polymer component such as poly(butyl methacrylate) and a second polymer component such as poly(ethylene-co-vinyl acetate).

Abstract: The present invention relates to a catheter systems for introducing and implanting an expandable stent member in a body. The catheter includes a catheter member having first and second ends, the first end having an inflatable portion, a lumen in fluid communication with the inflatable portion and the second end for inflating the inflatable portion. The expandable stent member is capable of permanent deformation when expanded. At least a portion of the stent member is attached to the inflatable portion by a bond and whereby upon inflation of the inflatable portion the bond is released from the stent member to permit deployment of the stent member and removal of the catheter member. The bond may be formed by the same or different material than the balloon surface. For example, an adhesive may be used.

Abstract: This is a surgical device particularly a perfusion catheter having an inflatable membrane or balloon located at the distal end of the catheter shaft. The catheter shaft is comprised of an outer tubing assembly and an inner tubing assembly separated by an open annulus for inflating and deflating the inflatable membrane. The assembly may additionally comprise an inflatable membrane which is detachable. The outer tubing assembly is made up of at least one polymeric layer and a braid which may be polymeric or metallic, perhaps of a super-elastic alloy. At least a portion of the inner tubing assembly is made up of at least one polymeric layer and preferably a super-elastic metallic braid. The inner tubing assembly includes a lumen through which a guidewire may pass. It is further desirable that the inner tubing assembly include a coil member which generally is coextensive with the balloon along its axis. That lumen is preferably lined with a lubricious polymer.

Abstract: A medical device for placing an embolic coil at a preselected location within a vessel comprising a positioning catheter having a distal tip for retaining the embolic coil which when pressurized with a fluid expands outwardly to release the coil at the preselected position and including an embolic coil having a relatively flexible proximal portion which resists stretching.

Abstract: The invention relates to coated stents and the method of making them. A stent that is substantially radiolucent is at least partially coated with a radiopaque layer that makes the stent visible under X-ray or fluoroscopy. A protective layer is coated on the stent and the radiopaque layer to protect both from scratches, flaking, and galvanic corrosion, and to improve both blood and bio-compatability.

Abstract: Methods are provided for inhibiting stenosis following vascular trauma or disease in a mammalian host, comprising administering to the host a therapeutically effective dosage of a therapeutic conjugate containing a vascular smooth muscle binding protein that associates in a specific manner with a cell surface of the vascular smooth muscle cell, coupled to a therapeutic agent dosage form that inhibits a cellular activity of the muscle cell. Methods are also provided for the direct and/or targeted delivery of therapeutic agents to vascular smooth muscle cells that cause a dilation and fixation of the vascular lumen by inhibiting smooth muscle cell contraction, thereby constituting a biological stent.

Abstract: A stent having varying outward radial force along its length. In use, the stent can provide greater force in vessel regions requiring greater force and less force in regions requiring less. In particular, more force is provided in the narrowed, center of a stenosis, while not applying too much force to the adjoining healthy tissue area. Greater stent expansion is provided in wider vessel geometries and less stent expansion in narrower regions. Varying force is achieved varying the number of elements, the density of elements, and the thickness of the elements.

Abstract: An endovascular graft having at least two barrier sections coupled to form a substantially tubular member. The barrier sections are coupled or connected to each other so as to allow relative axial displacement of the sections. The axial displacement of the barrier sections of the graft allows for a reduced profile and increased flexibility during delivery of the device to a desired site for deployment. The device may be delivered percutaneously or intraoperatively.

Abstract: An expandable reinforcing member or stent of the invention is used inside a body lumen, especially, in patient's artery for opening and holding a lesion or stenosis with a branch. The expandable reinforcing member is formed of at least two hollow mesh portions situated away from each other along an axial direction of the reinforcing member, and a connecting portion situated between the two hollow mesh porions for connecting the same. The connecting portion has a plurality of tortuous lines to define hollow areas therein, and a marker. Each hollow area is greater than a mesh size of the hollow mesh portions, and the marker is formed in one of the tortuous lines. Thus, a position of the connecting portion is realized at a time of installation of the reinforcing member. After the expandable reinforcing member is expanded, the reinforcing member can be slightly moved to relocate the position.

Abstract: A delivery system for implantation of a medical device in a body lumen including an elongate flexible catheter for delivering the medical device to a predetermined location in a lumen. The medical device surrounds the flexible catheter near its distal end and is held in a delivery configuration where the medical device has a reduced radius along its axial length by a storage sleeve. The storage sleeve surrounds the medical device. Where the catheter has an outer sleeve, the storage sleeve not only provides a means for retaining the medical device in its delivery configuration, but also protects the outer sleeve from creep during storage and/or elevated temperature conditions. The storage sleeve is removed from the system prior to use.

Abstract: A stent for implantation in a body vessel in which a cylindrical stent body coiled from a generally continuous wire with a zig-zag structure is provide with attachment of the wire ends to an adjacent coil.

Abstract: A welding method for improving the durability and strength of fusion weld joints in metal structures; the method is especially beneficial for metal structures fabricated from nickel-titanium alloy (nitinol) and for medical devices.

Abstract: An stent delivery device comprises a tubular shaft body, a foldable and inflatable balloon attached to the distal end portion of the shaft body, and a stent fitted over the folded balloon. The shaft body has a lumen for inflating the balloon which communicates with the inside of the balloon. The balloon has an inflatable portion which is inflated into the shape of an approximately uniform-diameter cylinder by a fluid injected through the lumen. The stent delivery device further has a distal side stopper which is secured close to the distal end of the inflatable portion of the balloon and prevents the shift of the stent toward the distal side, and a proximal side stopper which is secured close to the proximal end of the inflatable portion of the balloon and prevents the shift of the stent toward the proximal side.

Abstract: Tubular stents are formed from a sheet of material having longitudinally extending margins and an expandable pattern between the margins. The sheet can be formed to a tube with the margins overlapped and secured. The margins may be provided with means to facilitate registration of the margins.

Abstract: A stent for use in the treatment of stenosis of the ostium of tubular organs, more particularly, blood vessels comprising a multiplicity of flanges located at an end of a generally tubular stent body. The flanges permit the accurate positioning of the stent within the vessel, while presenting dislodgement of the stent.

Abstract: A method for occluding aneurysms or peripheral blood vessels is provided which allows for isovolumetric, isobaric delivery of occluding agents to aneurysms or peripheral blood vessels, wherein the aneurysms or peripheral blood vessels are isolated from the general circulation until the occluding agent has stabilized or until occlusion is effected. In particular, a double balloon method for occluding aneurysms or peripheral blood vessels is disclosed wherein a first balloon is inserted into the aneurysm or peripheral blood vessel to deliver an occluding agent, and a second balloon is placed such that it substantially covers the neck of the aneurysm or peripheral blood vessel to substantially seal the aneurysm or peripheral blood vessel from the general circulation. Additionally, an aneurysm or peripheral blood vessel comprising a double balloon configuration useful for occluding aneurysms or peripheral blood vessels is disclosed.

Abstract: An intraluminal stent comprising fibrin is capable of reducing the incidence of restenosis at the site of vascular injury such as that produced by an angioplasty procedure.

Abstract: An angioplasty and stent delivery system to facilitate introduction and placement of a stent, including a catheter having an expandable distal portion constructed and arranged for expanding the outer diameter of the catheter from a contracted state to an expanded state: a stent positioned around the distal portion of the catheter having a contracted condition and being expandable to an expanded condition, and being sized in the contracted condition to closely surround the catheter in the contracted state, the expandable distal portion of the catheter including a balloon within which or over which there is included on a catheter shaft at least one axially movable or enlargeable body of a diameter larger than the catheter shaft to which the stent and balloon are fitted, as by crimping, for holding the stent in place until it is released therefrom by expansion of the balloon.

Abstract: A stent for reinforcing a vessel wall is disclosed, the stent being expandable and comprised of a shape memory alloy which in the normal implanted condition is in the martensitic phase at body temperature, the stent further having a larger parent or austenitic shape and diameter when heated above its transition temperature.

Abstract: A surgical dissecting retractor for harvesting vascular conduits or vessels such as saphenous veins and the like is disclosed which dissects tissue and top and/or side branches from the vessel as it is advanced along a desired segment of the vessel via an entry incision in a patient's skin. The dissecting retractor is inserted while in a closed or "low profile" position to minimize trauma to the vessel and patient. Once installed above the vessel, the retractor is opened and locked to present a relatively "high profile", thereby creating and maintaining an enlarged working space or tunnel in the region between the skin and the vessel being harvested. Completion of the vessel harvesting procedure proceeds with suitable surgical instruments for dissecting, ligating, cauterizing and/or clipping, with or without visualizing devices which comprise further adjunct features of the retractors in accordance with the invention.

Abstract: A bifurcated endovascular stent is formed from a pair of individual tubular component stents that can be placed independently in sequence in the branched region of a body vessel to form the bifurcated stent in situ. The first placed component stent includes a side opening and may be placed to extend both proximally and distally of the bifurcated junction with the side opening facing the entry to the branch vessel. The first component stent then is expanded within the vessel. The second component stent then can be advanced through the first component stent, through the side opening and into the branch vessel where it can be expanded. The portions of the first and second component stents that surround the region of the vessel juncture are constructed to provide enhanced lateral support for the walls of the vessel in the region of the junction.

Abstract: A flexible stent is provided that has features to minimize recoil and facilitate anchoring of the stent in a vascular passage. The design features sharp angulated bends. Other features include a rounded cross-section in the wire or stent components. Another feature is the bending of the angulated bends in a transverse plane to provide additional rigidity and an anchoring mechanism. Ties are provided in alignment or in staggered fashion, either semi-rigid or flexible, to allow the structure, which can be made of joined rings or a helical arrangement, to be more flexible to accommodate bends in the vascular system. The ties are also disclosed with a locking system involving bending the wire as it is formed into a helix in combination with crossties with loops which lock the stent in an expanded position.

Abstract: A luminal endoprosthesis comprising a framework made up of braided filaments. The framework is self-expanding, that is to say that after it has been radially compressed for positioning of the endoprosthesis, it automatically recovers its nominal diameter. The metal of the framework has undergone a thermal treatment bringing about a state transition, at a temperature close to that of the organism, and this confers upon it a suitable rigidity after it has been positioned in an anatomical conduit.

Abstract: A body tissue graft for use in a patient includes a frame structure made of a first elastic material, a covering of a second elastic material on the frame structure, the covering substantially filling openings in the frame structure, and a connector connected to the frame structure. Projections are secured to the connector structure. The projections facilitate attachment of the tubular graft in a patient by securing the graft to the body tissue with which the graft is employed. The connector selectively circumferentially expands and the projections selectively circumferentially expand. This may be done using an inflatable balloon to circumferentially expand the projections. A restraining member may be provided to restrain the projections in a cone shape so that an end of the graft may be used to open an aperture through a side wall of existing body organ tubing and a portion of the projections may enter the aperture.

Abstract: A radially expandable stent which is formed from a fine wire bent into a serpentine flat ribbon which is wound around a mandrel into a cylindrical sleeve for mounting on a balloon catheter for transluminal insertion in a vessel. The wire forming the stent comprises an alloy selected from the group consisting of Pt--Ir or Au--Ni, and where the alloy exhibits a tensile strength of about 155,000 to 175,000 PSI.

Abstract: The device comprises a prosthesis designed as a hollow body compressed against the action of restoring spring forces to a cross section reduced relative to an expanded use position, and held in this position by a strippable sheath. After the sheath is stripped, the prosthesis automatically expands to a cross section corresponding to the use position. The sheath, which can be a meshwork in the approximate form of crocheted material, extends over the entire length of the prosthesis and consists of at least one continuous thread and at least one drawstring. The prosthesis, held in the radially compressed position by the sheath, can be mounted displaceably on a feed wire or non-axially-displaceably on the insertion end of a probe or a catheter.

Abstract: An intraluminal grafting system includes a hollow graft which has a proximal staple positioned proximate its proximal end and a distal staple adapted proximate its distal end. The system includes a capsule for transporting the graft through the lumen and for positioning the proximal end of the graft upstream in a lumen which may be a blood vessel or artery. A tube is connected to the capsule and extends to exterior the vessel for manipulation by the user. A catheter is positioned within the tube to extend from the cavity and through the graft to exterior the body. The catheter has an inflatable membrane or balloon proximate the distal end thereof which is in communication via a channel with inflation and deflation means located exterior the vessel. With the inflatable membrane deflated, the capsule is positioned in the lumen and manipulated to a desired location. The inflatable mabrane is manipulated by the rod away from the graft.

Abstract: An intraluminal prosthesis for intraluminal repair of body conduits, especially aortic aneurysms, is disclosed. The prosthesis includes a generally tubular, flexible graft (20) having a proximal open end (30) and at least one distal open end (31) terminating in a hem (33). A stent (21) can be disposed within the proximal open end (30) and is adapted to be attached to the body conduit (1). The hem (33) is inverted within the graft so that it is disposed as a cuff (34) within the graft. The hem (33) is arranged so that upon withdrawing the distal open end (31) from inside the cuff (34), the cuff will unfold and follow the distal open end to expose it to receive another stent for attachment to the body conduit (12) for intraluminal implantation of the graft. Preferably the hem is folded a second time within the cuff to form a second cuff (35) within the graft. The stents are preferably formed of a plexus of wires adapted to expand from a first narrow diameter to a second diameter to engage the body conduit.

Abstract: A radially expandable support body is enveloped within a cocoon. In a preferred construction, the support is a stent, and a tube of polymeric material, e.g. polytetrafluoroethylene (PTFE), passes through the interior of the stent body and is turned back upon itself over the stent to form a cuff. The assembly is then heated and the outer layer contacts and coalesces with the inner layer, closely surrounding the stent body within a folded envelope having a continuous and seamless end. In one embodiment, an end portion of the tube is expanded before folding back over the stent. The end portion, which becomes an exterior surface of the finished product, thus acquires a greater degree of porosity. Each end of the central tube may be so expanded, and folded back to seal all surfaces and both ends. The stent body itself may be a ring, or a short series of spaced-apart rings, or a wire or web, or a sheet possessing a number of apertures extending entirely through the sheet.

Abstract: The present invention provides a catheter apparatus, an improved introducer system, and a methodology for creating a bypass on-demand between an unobstructed blood vessel such as the aorta and an obstructed blood vessel such as an obstructed coronary artery in-vivo using a prepared shape-memory alloy cuff and a graft segment in tandem as a shunt. The invention allows the placement and creation of single or multiple bypass grafts without use of a heart-lung machine and without need for stopping the heart of the patient during the coronary artery bypass surgery.

Abstract: An inflatable intraluminal stent for attachment to the interior surface of a tubular structure within the human body is disclosed. The stent features a cuff having an inflatable chamber and a friction-enhancing outer surface. The friction-enhancing outer surface engages the interior surface of the tubular structure without penetration when the inflatable cuff is in an inflated condition. An intraluminal medical device may be attached to the inner surface of the stent. A valve is integral with the inflatable cuff and allows for the inflation, deflation and sealing of the inflatable cuff.

Abstract: A stent delivery system to facilitate introduction and placement of a stent, including a catheter having an expandable distal portion constructed and arranged for expanding the outer diameter of the catheter from a contracted state to an expanded state: a stent positioned around the distal portion of the catheter having a contracted condition and being expandable to an expanded condition, and being sized in the contracted condition to closely surround the catheter in the contracted state, the expandable distal portion of the catheter including a balloon within which there is included on the catheter shaft at least one body of a diameter larger than the catheter shaft to which the stent and balloon are fitted, as by crimping, for holding the stent in place until it is released therefrom by expansion of the balloon.

Abstract: The invention is directed to a prosthetic device comprising a support member comprising a stent, a conduit or a scaffold; and a layer of elastin or elastin-based material located on said support member. Preferably, the layer of said elastin or elastin-based biomaterial completely surrounds said support member. The support member can be formed of a metal or a synthetic material such as a polymeric material.

Abstract: A stent delivery system to facilitate introduction and placement of a stent, including a catheter having an expandable distal portion constructed and arranged for expanding the outer diameter of the catheter from a contracted state to an expanded state: a stent positioned around the distal portion of the catheter having a contracted condition and being expandable to an expanded condition, and being sized in the contracted condition to closely surround the catheter in the contracted state, the expandable distal portion of the catheter including a balloon within which there is included on the catheter shaft at least one body of a diameter larger than the catheter shaft to which the stent and balloon are fitted, as by crimping, for holding the stent in place until it is released therefrom by expansion of the balloon.

Abstract: An intraluminal, crush resistant stent for implantation in a body lumen is disclosed. The crush resistant stent is made from a base section having a plurality of resilient, parallel, coplanar struts having a zig-zag configuration extending therefrom wherein the zig-zag struts are curved and pass through corresponding slots in the base section to form a continuous, cylindrical hoop. Each zig-zag strut has an amplitude that decreases when the zig-zag strut is placed under tension and an amplitude that increases when the zig-zag strut is unstressed or is placed under compression. Accordingly, each zig-zag strut can be pulled through the respective slot in the base section, but under compression the zig-zag struts assume the larger amplitude and cannot pass through the corresponding slot thereby maintaining the diameter of the stent constant.