Abstract: A system for containment and organization of a medical wire features a clamp. A first ridged and grooved clamping block is located on a clamp first side posterior end and a second ridged and grooved clamping block is located on a clamp second side posterior end. A first side compression member is located on an inside surface of a clamp first side and a second side compression member is located on an inside surface of the clamp second side. An adjustable ratcheting lock attaches the clamp first side and the clamp second side. A first finger grip is located on an outside surface of the clamp first side and a second finger grip is located on an outside surface of the clamp second side. A Medical wire is placed between the first side compression member and the second side compression member then the clamp is compressed against the medical wire.

Abstract: A system for containment and organization of a medical wire features a clamp. A first ridged and grooved clamping block is located on a clamp first side posterior end and a second ridged and grooved clamping block is located on a clamp second side posterior end. A first side compression member is located on an inside surface of a clamp first side and a second side compression member is located on an inside surface of the clamp second side. An adjustable ratcheting lock attaches the clamp first side and the clamp second side. A first finger grip is located on an outside surface of the clamp first side and a second finger grip is located on an outside surface of the clamp second side. A Medical wire is placed between the first side compression member and the second side compression member then the clamp is compressed against the medical wire.

Abstract: A system for containment and organization of a medical wire features a clamp. A first ridged and grooved clamping block is located on a clamp first side posterior end and a second ridged and grooved clamping block is located on a clamp second side posterior end. A first side compression member is located on an inside surface of a clamp first side and a second side compression member is located on an inside surface of the clamp second side. An adjustable ratcheting lock attaches the clamp first side and the clamp second side. A first finger grip is located on an outside surface of the clamp first side and a second finger grip is located on an outside surface of the clamp second side. A Medical wire is placed between the first side compression member and the second side compression member then the clamp is compressed against the medical wire.

Abstract: A system for containment and organization of a medical wire features a clamp. A first ridged and grooved clamping block is located on a clamp first side posterior end and a second ridged and grooved clamping block is located on a clamp second side posterior end. A first side compression member is located on an inside surface of a clamp first side and a second side compression member is located on an inside surface of the clamp second side. An adjustable ratcheting lock attaches the clamp first side and the clamp second side. A first finger grip is located on an outside surface of the clamp first side and a second finger grip is located on an outside surface of the clamp second side. A Medical wire is placed between the first side compression member and the second side compression member then the clamp is compressed against the medical wire.

Abstract: A system for containment and organization of a medical wire features a clamp. A first ridged and grooved clamping block is located on a clamp first side posterior end and a second ridged and grooved clamping block is located on a clamp second side posterior end. A first side compression member is located on an inside surface of a clamp first side and a second side compression member is located on an inside surface of the clamp second side. An adjustable ratcheting lock attaches the clamp first side and the clamp second side. A first finger grip is located on an outside surface of the clamp first side and a second finger grip is located on an outside surface of the clamp second side. A Medical wire is placed between the first side compression member and the second side compression member then the clamp is compressed against the medical wire.

Abstract: Prosthetic valve devices for implantation in body vessels are provided. The prosthetic valve device includes at least one flexible member that permits fluid flow in a first direction and substantially prevents fluid flow in a second. The valve device also includes an inflatable chamber at least partially attached to the flexible member. The inflatable chamber is adapted to receive inflating media and is adapted to contact the body vessel. A delivery system is also provided that includes a valve device and a delivery apparatus. The delivery apparatus includes a member adapted for filling the chamber of the valve device with inflating media. A related method of making the valve device is also provided.

Abstract: Prosthetic valve devices for implantation in body vessels are provided. The prosthetic valve device includes at least one flexible member that permits fluid flow in a first direction and substantially prevents fluid flow in a second. The valve device also includes an inflatable chamber at least partially attached to the flexible member. The inflatable chamber is adapted to receive inflating media and is adapted to contact the body vessel. A delivery system is also provided that includes a valve device and a delivery apparatus. The delivery apparatus includes a member adapted for filling the chamber of the valve device with inflating media. A related method of making the valve device is also provided.

Abstract: A medical device including a guiding member and a filter portion is disclosed. The guiding member includes a lumen configured to slidably engage the filter portion. The filter portion forms a tubular geometry that extends distally from the guiding member. The filter portion is configured to evert to form a proximally facing concave geometry for capturing emboli. Further, the filter portion includes filter openings that are sized to allow blood cells to pass therethrough while preventing the passage of emboli.

Abstract: The present invention provides a wire guide having a variable stiffness region that may be selectively adjusted to vary the stiffness along a portion of the wire guide. The wire guide generally comprises an outer core member and an inner core member, wherein the inner core member is disposed for longitudinal movement with respect to the outer core member. The outer core member is attached to a proximal end of a coiled member, while the inner core member is attached to the coiled member at an attachment region between proximal and distal ends of the coiled member. In operation, distal advancement of the outer core member with respect to the inner core member causes the coiled member to compress at a location between the proximal end of the coiled member and the attachment region, thereby selectively increasing the stiffness along a portion of the length of the wire guide.

Abstract: Prosthetic valve devices for implantation in body vessels are provided. The prosthetic valve device includes at least one flexible member that permits fluid flow in a first direction and substantially prevents fluid flow in a second. The valve device also includes an inflatable chamber at least partially attached to the flexible member. The inflatable chamber is adapted to receive inflating media and is adapted to contact the body vessel. A delivery system is also provided that includes a valve device and a delivery apparatus. The delivery apparatus includes a member adapted for filling the chamber of the valve device with inflating media. A related method of making the valve device is also provided.

Abstract: A balloon catheter assembly included a catheter provided with a distal end and a proximal end and at least one inflation lumen in the catheter. The inflation lumen includes a distal end and a proximal end. An inflatable balloon is provided at the distal end of the catheter and in fluid communication with the distal end of said inflation lumen. The proximal end of the inflation lumen is able to be coupled to a source of fluid. A flow controller is coupled between the inflation lumen and the fluid source, the flow controller being adjustable by an operator of the balloon catheter assembly so as to adjust the flow of inflation fluid to the balloon. In one embodiment, the flow controller includes a manually operable control actuator and a plurality of discrete flow configurations provided in the form of flow through holes in the flow controller.

Abstract: The present invention provides a wire guide having a variable stiffness region that may be selectively adjusted to vary the stiffness along a portion of the wire guide. The wire guide generally comprises an outer core member and an inner core member, wherein the inner core member is disposed for longitudinal movement with respect to the outer core member. The outer core member is attached to a proximal end of a coiled member, while the inner core member is attached to the coiled member at an attachment region between proximal and distal ends of the coiled member. In operation, distal advancement of the outer core member with respect to the inner core member causes the coiled member to compress at a location between the proximal end of the coiled member and the attachment region, thereby selectively increasing the stiffness along a portion of the length of the wire guide.

Abstract: An occlusion device for occluding a body vessel. The occlusion device includes a first hub extending from a proximal end to a distal end and a tubular wall defining a lumen having a central axis. A plurality of arcuate legs are attached to the first hub and extend distally to a distal portion. The legs extend radially away from the central axis in an open configuration and extend substantially along the central axis in a closed configuration. A biocompatible material is attached to the plurality of legs to form an occlusive barrier when deployed within the body vessel. The biocompatible material either extends along and between each of the plurality of legs or it forms a disk attached to at least one leg.

Abstract: A rapid exchange assembly comprises an introducer sheath, and a dilator receivable within a lumen of the introducer sheath. The dilator has an open distal end and a lumen extending therein. A distal portion of the dilator extends distally beyond the distal end of the introducer sheath when the dilator is received in the lumen of the introducer sheath. The dilator has an opening through a wall in the distal portion which communicates with the open distal end of the dilator. A wire guide is receivable through the open distal end of the dilator and extends through the opening in the distal portion of the dilator outwardly of the assembly along the length of the introducer sheath.

Abstract: A medical device including a guiding member and a filter portion is disclosed. The guiding member includes a lumen configured to slidably engage the filter portion. The filter portion forms a tubular geometry that extends distally from the guiding member. The filter portion is configured to evert to form a proximally facing concave geometry for capturing emboli. Further, the filter portion includes filter openings that are sized to allow blood cells to pass therethrough while preventing the passage of emboli.

Abstract: A method and device to repair a stenosis in a blood vessel is provided. The medical device has a tubular member and a frame. The frame may be expanded or contracted while maintaining its generally cylindrical configuration. The medical device is retained in a contracted state inside an introducer sheath. The introducer sheath is guided through the stenosis such that a first end of the medical device is located distal the stenosis. The introducer sheath is retracted relative to the medical device, such that the first end of the stent expands to engage the blood vessel distal the stenosis. A mid-portion of the medical device engages the plaque of the stenosis trapping any emboli against the wall of the vessel. The second end expands to engage the blood vessel proximal to stenosis.

Abstract: Prosthetic valve devices for implantation in body vessels are provided. The prosthetic valve device includes at least one flexible member that permits fluid flow in a first direction and substantially prevents fluid flow in a second. The valve device also includes an inflatable chamber at least partially attached to the flexible member. The inflatable chamber is adapted to receive inflating media and is adapted to contact the body vessel. A delivery system is also provided that includes a valve device and a delivery apparatus. The delivery apparatus includes a member adapted for filling the chamber of the valve device with inflating media. A related method of making the valve device is also provided.