Abstract: An implantable stent forming a tubular scaffolding including a plurality of individual struts arranged in a pattern defining open spaces. The tubular scaffolding with a lumen defined therethrough having a lumen facing surface facing radially inward toward the lumen and an opposite tissue facing surface facing radially outward away from the lumen. Each individual strut has a longitudinal axis and a lateral cross-section with opposing sides extending between the lumen facing surface and the tissue facing surface. Furthermore, at least one structural extension member associated with one of the individual struts, wherein the structural extension member extends in a direction perpendicular to the longitudinal axis outward from one of the opposing sides of the associated individual strut and the structural extension member has a plurality of growth promoting structural elements.

Abstract: A method of treating an aneurysm, including determining a diameter associated with a vessel having the aneurysm; selecting one of a plurality of braided implants for treating the vessel, wherein each braided implant comprises a porosity substantially consistent over up to a 1 mm diameter range, each braided implant configured to provide consistent porosity over different diameter ranges; and treating the vessel with the one of the plurality of braided implants.

Abstract: A vascular flow diverter includes a tubular mesh framework which includes a mesh cover and an opening. The tubular mesh framework is collapsible and configured to expand from a collapsed shape to a tubular shape when the vascular flow diverter is deployed. The mesh cover conforms to the shape of the tubular mesh, is surrounded by the tubular mesh framework, and is less porous than the tubular mesh framework. The opening is located within the mesh cover. A delivery wire passes through the opening in order to guide the flow diverter into place over an aneurysm.

Abstract: The disclosed technology generally relates to braided implants for aneurysm therapy. The disclosed technology can include a system having a tubular braid comprising an open end, a pinched end, and a predetermined shape. In the predetermined shape, the tubular braid can include a first segment extending from the open end to a first inversion, a second segment extending from the first inversion to a second inversion and forming a bag comprising a semi-frustoconically-shaped portion proximate the first inversion such that the semi-frustoconically-shaped portion defines an inner channel forming an opening to the bag, and a third segment surrounded by the second segment and extending from the second inversion to the pinched end. The system can include a catheter having a lumen therethrough, a distal end, and an outer diameter at the distal end being sized to be inserted into the bag through the opening of the bag.

Abstract: Delivery and detachment system for an implantable intravascular treatment device, the system including an outer delivery tube and a proximal inner tube telescopically slidable within the lumen of the outer delivery tube. The proximal inner tube has a weld window radially inward cutout defined therein along an axial section between the proximal and distal ends. A securement wire disposed axially within the lumen of the proximal inner tube is secured to an inner wall of the lumen of the proximal inner tube via at least one supplemental connection point coinciding with the weld window. Also, the method for making the delivery and detachment system wherein one or more positioning wires threaded through the lumen of the proximal inner tube are manipulated to force the securement wire and the proximal inner tube in direct physical contact with one another along an axial section coinciding with the weld window.

Abstract: A detachment system for delivering an embolic coil implant to a treatment site is provided. A loop wire that is looped over a pull wire of the system can include one or more twists to increase frictional resistance against the pull wire. The additional resistance decreases likelihood of premature deployment of the embolic coil prior to the detachment system reaching the treatment site.

Abstract: Delivery and detachment system for an implantable intravascular treatment device, the system including an outer delivery tube and a proximal inner tube telescopically slidable within the lumen of the outer delivery tube. The proximal inner tube has a weld window radially inward cutout defined therein along an axial section between the proximal and distal ends. A securement wire disposed axially within the lumen of the proximal inner tube is secured to an inner wall of the lumen of the proximal inner tube via at least one supplemental connection point coinciding with the weld window. Also, the method for making the delivery and detachment system wherein one or more positioning wires threaded through the lumen of the proximal inner tube are manipulated to force the securement wire and the proximal inner tube in direct physical contact with one another along an axial section coinciding with the weld window.

Abstract: A self-expanding braided stent includes at least a distal radial expansion ring added to a distal end of the stent body to increase a radial expansion force of the self-expanding braided stent in deployment of the stent, and to facilitate advancement of the stent through a delivery sheath by a core advancement wire. A proximal radial expansion ring is optionally added to a proximal end of the stent body to allow the stent to be recaptured following partial deployment by retraction of the core advancement wire, prior to full deployment of a proximal portion of the stent body.

Abstract: A method is disclosed, including joining a balloon to a resilient inner body of a balloon assist device, the balloon comprising an axial length shorter than an axial length of the inner body; expanding a slit in the resilient inner body of the balloon assist device; inserting a catheter through the slit; and releasing the slit to contract the balloon assist device around the catheter.

Abstract: A self-expanding braided stent includes at least a distal radial expansion ring added to a distal end of the stent body to increase a radial expansion force of the self-expanding braided stent in deployment of the stent, and to facilitate advancement of the stent through a delivery sheath by a core advancement wire. A proximal radial expansion ring is optionally added to a proximal end of the stent body to allow the stent to be recaptured following partial deployment by retraction of the core advancement wire, prior to full deployment of a proximal portion of the stent body.

Abstract: An implant can be placed into an aneurysm sac that includes a bioabsorbable coiled fiber having a coiled shape similar to a metallic embolic coil. The implant can have an absorption rate long enough so that the aneurysm can become sufficiently occluded and sufficiently healed as the implant is absorbed. The implant can include crossing microfibers to initiate thrombosis within the aneurysm and/or a stretch-resistant member extending through a lumen of the coiled shape to inhibit elongation of the coiled shape. The crossing microfibers can be attached to the coiled fiber by friction fit between coil windings, heat bonding to the coiled fiber, and/or securement to the stretch-resistant member. The coiled fiber, crossing microfibers, and stretch-resistant member can have rates of absorption that differ to promote an accelerated sequence of occlusion and healing of the aneurysm.

Abstract: An occlusion device that includes an inner embolic element with a proximal section and a distal section, wherein the distal section has a first stiffness and the proximal section has a second stiffness. An expandable mesh is included that is capable of being transformed between a collapsed position and an expanded position, wherein the expandable mesh is disposed over a portion of the proximal section of the inner embolic device and the first stiffness is greater than the second stiffness.

Abstract: A self-expanding braided stent includes at least a distal radial expansion ring added to a distal end of the stent body to increase a radial expansion force of the self-expanding braided stent in deployment of the stent, and to facilitate advancement of the stent through a delivery sheath by a core advancement wire. A proximal radial expansion ring is optionally added to a proximal end of the stent body to allow the stent to be recaptured following partial deployment by retraction of the core advancement wire, prior to full deployment of a proximal portion of the stent body.

Abstract: A generally tubular braided flow diverting stent is formed of alternating round and rectangular elongated members, for treatment of aneurysms. The generally tubular braided flow diverting stent maintains a significant wall thickness while increasing area coverage of a vessel wall. Sliding of the round elongated members over the rectangular elongated members allows the stent to be crimped to very low diameters for delivery in narrow portions of the vasculature.

Abstract: An occlusion device that includes an inner embolic element with a proximal section and a distal section, wherein the distal section has a first stiffness and the proximal section has a second stiffness. An expandable mesh is included that is capable of being transformed between a collapsed position and an expanded position, wherein the expandable mesh is disposed over a portion of the proximal section of the inner embolic device and the first stiffness is greater than the second stiffness.

Abstract: A method of treating an aneurysm, including determining a diameter associated with a vessel having the aneurysm; selecting one of a plurality of braided implants for treating the vessel, wherein each braided implant comprises a porosity substantially consistent over up to a 1 mm diameter range, each braided implant configured to provide consistent porosity over different diameter ranges; and treating the vessel with the one of the plurality of braided implants.

Abstract: A method of treating an aneurysm, including determining a diameter associated with a vessel having the aneurysm; selecting one of a plurality of braided implants for treating the vessel, wherein each braided implant comprises a porosity substantially consistent over up to a 1 mm diameter range, each braided implant configured to provide consistent porosity over different diameter ranges; and treating the vessel with the one of the plurality of braided implants.

Abstract: An occlusion device that includes an inner embolic element with a proximal section and a distal section, wherein the distal section has a first stiffness and the proximal section has a second stiffness. An expandable mesh is included that is capable of being transformed between a collapsed position and an expanded position, wherein the expandable mesh is disposed over a portion of the proximal section of the inner embolic device and the first stiffness is greater than the second stiffness.

Abstract: An implant that includes a plurality of only single strands with at least a first non-radiopaque material and at least one multi-strand of radiopaque material among the single strands, the multi-strand including at least two side-by-side radiopaque filaments contiguous to each other over a length of the multi-strand.

Abstract: A vascular flow diverter includes a tubular mesh framework which includes a mesh cover and an opening. The tubular mesh framework is collapsible and configured to expand from a collapsed shape to a tubular shape when the vascular flow diverter is deployed. The mesh cover conforms to the shape of the tubular mesh, is surrounded by the tubular mesh framework, and is less porous than the tubular mesh framework. The opening is located within the mesh cover. A delivery wire passes through the opening in order to guide the flow diverter into place over an aneurysm.