Abstract: Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts Po. in a central portion of the winding between the ends of the winding.

Abstract: A surgical retention port particularly useful as an arthroscopic port for shoulder surgery is provided. The surgical retention port has an inner cannula defining a throughbore, a plurality of rotatable fingers coupled to the inner cannula, and an outer cannula extending around the inner cannula. Rotation of the inner cannula relative to the outer cannula causes the rotation of the fingers from a first position where the fingers assume a collapsed configuration to a second position where the fingers assume an extended or open configuration.

Abstract: Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have five extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts in a central portion of the winding between the ends of the winding.

Abstract: A stent includes a stent body having a circumference and struts disposed helically about the circumference. Each of the struts has a strut length and a ratio of a number of the struts around the circumference to the strut length is greater than 800 per inch, in particular, over 1000 per inch. A method for manufacturing a helical stent includes the steps of providing a stent body with struts disposed about the circumference thereof in turns and with bridges connecting the struts in adjacent turns. The stent body is expanded and, thereafter, some of the bridges, in particular, sacrificial bridges, are removed.

Abstract: A stent includes a stent body having a circumference, a diameter of between approximately 4 mm and approximately 12 mm, in particular, 8 mm, and a length of between approximately 10 mm and approximately 250 mm, in particular, 150 mm, and struts disposed helically about the circumference in turns. Substantially circumferentially oriented connecting bridges connect respectively adjacent ones of the turns. A method for manufacturing a helical stent includes the steps of providing a stent body with struts disposed about the circumference thereof in turns and with bridges connecting the struts in adjacent turns. The stent body is expanded and, thereafter, some of the bridges, in particular, sacrificial bridges, are removed.

Abstract: Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding and at least one bridge. The continuous helical winding has a plurality of circumferential sections that circumscribe a longitudinal axis from a first end to a second end to define a tube. The circumferential sections are spaced apart along the axis. The at least one bridge is configured to connect one circumferential section to an axially-spaced adjacent circumferential section. The at least one bridge extends on a plane generally orthogonal with respect to the axis.

Abstract: Methods and apparatus for treating the interior of a blood vessel include a variety of improved catheter designs, methods and apparatus for accessing and occluding a blood vessel.

Abstract: The methods of the invention include examining a blood vessel to be treated, preferably with the aid of ultrasound, calculating a volume of the portion of the blood vessel, and treating the portion with a volume of treatment agent where the volume of treatment agent is a function of the volume of the portion of the blood vessel. Apparatus for implementing the methods are provided.

Abstract: An implantable radiation therapy device includes a biocompatible radiotranslucent outer capsule containing a radiation shielding element and a radioactive isotope at least partially shielded by the shielding element. When the device is at or below body temperature, radiation is prevented or limited from being transmitted through the outer capsule by the shielding element. When non-ambient energy is applied to the device, the shielding element and radioactive isotope are reconfigured such that an increased level of radiation is transmitted through the outer capsule and emitted by the device.

Abstract: A stent includes a marker mount defined by a pair of fingers. The fingers are preferably oriented parallel to the longitudinal axis of the stent. The fingers preferably each include a retainer at their respective ends, and the retainers of each pair of fingers preferably define a composite barb. A tubular marker can be forced over the bifurcated barb and onto the fingers. The marker is preferably provided with a ceramic coating to prevent galvanic corrosion between the stent and the marker.

Abstract: Radioactive therapeutic seeds include one or more carrier structures each carrying a radioactive isotope, a ceramic spacer or collar member, a metal ring about the ceramic member, and a capsule formed from two tubular parts, each part including a closed end, an open end, and an interior. The open ends of the capsule abut the metal ring and are preferably welded thereto to form a generally uniform capsule wall such that the carrier structure(s) and ceramic member are contained in the interior of the capsule. The ceramic spacer preferably is hollow and a radiopaque or MRI-visible marker extends therethrough. Each of the embodiments is designed to provide a substantially isotropic distribution of radiation.

Abstract: A process for creating surface microporosity on a titanium (or other metal) medical device includes creating a surface oxide layer on the device; placing the device, which is connected to a negative terminal of an electrical power supply, into a calcium chloride bath; connecting the positive terminal of the power supply to an anode immersed in or containing calcium chloride thereby forming an electrolytic cell; passing current through the cell; removing the device from the bath; and cooling and rinsing the device to remove any surface salt. If necessary, the device is etched to remove metal oxide which may have formed during the cooling process. The resulting device has a microporous surface structure. Alternatively, only a designated surface portion of a medical device is made microporous, either by applying a non-oxidizing mask, removing a portion of the oxide layer, or subtracting a portion of a microporous surface.

Abstract: An implantable radiation therapy device includes a biocompatible radiotranslucent outer capsule containing a radiation shielding element and a radioactive isotope at least partially shielded by the shielding element. When the device is at or below body temperature, radiation is prevented or limited from being transmitted through the outer capsule by the shielding element. When non-ambient energy is applied to the device, the shielding element and radioactive isotope are reconfigured such that an increased level of radiation is transmitted through the outer capsule and emitted by the device.

Abstract: Radioactive therapeutic seeds include one or more carrier structures each carrying a radioactive isotope, a ceramic spacer or collar member, a metal ring about the ceramic member, and a capsule formed from two tubular parts, each part including a closed end, an open end, and an interior. The open ends of the capsule abut the metal ring and are preferably welded thereto to form a generally uniform capsule wall such that the carrier structure(s) and ceramic member are contained in the interior of the capsule. The ceramic spacer preferably is hollow and a radiopaque or MRI-visible marker extends therethrough. Each of the embodiments is designed to provide a substantially isotropic distribution of radiation.

Abstract: A process for creating surface microporosity on a titanium (or other metal) medical device includes creating a surface oxide layer on the device; placing the device, which is connected to a negative terminal of an electrical power supply, into a calcium chloride bath; connecting the positive terminal of the power supply to an anode immersed in or containing calcium chloride thereby forming an electrolytic cell; passing current through the cell; removing the device from the bath; and cooling and rinsing the device to remove any surface salt. If necessary, the device is etched to remove metal oxide which may have formed during the cooling process. The resulting device has a microporous surface structure. Alternatively, only a designated surface portion of a medical device is made microporous, either by applying a non-oxidizing mask, removing a portion of the oxide layer, or subtracting a portion of a microporous surface.

Abstract: A process for creating surface microporosity on a titanium (or other metal) medical device includes creating a surface oxide layer on the device; placing the device, which is connected to a negative terminal of an electrical power supply, into a calcium chloride bath; connecting the positive terminal of the power supply to an anode immersed in or containing calcium chloride thereby forming an electrolytic cell; passing current through the cell; removing the device from the bath; and cooling and rinsing the device to remove any surface salt. If necessary, the device is etched to remove metal oxide which may have formed during the cooling process. The resulting device has a microporous surface structure. Alternatively, only a designated surface portion of a medical device is made microporous, either by applying a non-oxidizing mask, removing a portion of the oxide layer, or subtracting a portion of a microporous surface.

Abstract: Radioactive therapeutic seeds include one or more carrier structures each carrying a radioactive isotope, a ceramic spacer or collar member, a metal ring about the ceramic member, and a capsule formed from two tubular parts, each part including a closed end, an open end, and an interior. The open ends of the capsule abut the metal ring and are preferably welded thereto to form a generally uniform capsule wall such that the carrier structure(s) and ceramic member are contained in the interior of the capsule. The ceramic spacer preferably is hollow and a radiopaque or MRI-visible marker extends therethrough. Each of the embodiments is designed to provide a substantially isotropic distribution of radiation.

Abstract: An implantable radiation therapy device includes a biocompatible radiotranslucent outer capsule containing a radiation shielding element and a radioactive isotope at least partially shielded by the shielding element. When the device is at or below body temperature, radiation is prevented or limited from being transmitted through the outer capsule by the shielding element. When non-ambient energy is applied to the device, the shielding element and radioactive isotope are reconfigured such that an increased level of radiation is transmitted through the outer capsule and emitted by the device.

Abstract: Radioactive therapeutic seeds include one or more carrier structures each carrying a radioactive isotope, a ceramic spacer or collar member, a metal ring about the ceramic member, and a capsule formed from two tubular parts, each part including a closed end, an open end, and an interior. The open ends of the capsule abut the metal ring and are preferably welded thereto to form a generally uniform capsule wall such that the carrier structure(s) and ceramic member are contained in the interior of the capsule. The ceramic spacer preferably is hollow and a radiopaque or MRI-visible marker extends therethrough. Each of the embodiments is designed to provide a substantially isotropic distribution of radiation.

Abstract: Radioactive therapeutic seeds include a substantially radiotransparent cylindrical capsule containing a radioactive isotope and, in particular embodiments, a radiopaque or MRI-visible marker. Each of the embodiments is designed to provide a substantially isotropic distribution of radiation. In one embodiment, the isotope is deposited on the outer surface of a hollow radiolucent tube and a collar is provided about a central portion of the tube. The capsule comprises two tubular halves positioned over the tube with the open ends of the halves forming an interference fit with the collar and welded thereabout. In another embodiment, the isotope bearing structure is a plurality of radiolucent spheres provided with a thin coating of silver to facilitate the adhesion of the isotope thereto. The spheres are provided in two capsule halves which are welded closed about a plug have an axial radiopaque marker therein.