An aortic root replacement device is movable between a deployed configuration and a retracted configuration. The device includes an intraventricular stent having a proximal portion and a distal portion, the intraventricular stent is flared from the proximal portion towards the distal portion such that when the device is deployed in the ventricle below the aortic valve it is held in position in the ventricle. The device also includes—an aortic valve unit and an aortic stent extending from the intraventricular stent. The intraventricular stent, the aortic valve unit and the aortic stent form a unitary assembly in retracted configuration and in deployed configuration, the aortic stent includes at least three means for connecting the device to the coronary arteries.

A bioabsorbable implant including an elongated metallic element having more than 50% by weight a metal and being substantially free of rare earth elements, the elongated metallic element defining at least a portion of the bioabsorbable implant and including a wire formed into a discrete bioabsorbable expandable metal ring; at least two biostable ring elements, each biostable ring element having a biostable and radio-opaque metallic alloy, the bioabsorbable expandable metal ring being disposed adjacent to at least one of the biostable ring elements; at least one flexible longitudinal connector including a bioabsorbable polymer, the connector being disposed between at least two adjacent rings; and a coating having at least one pharmaceutically active agent disposed over at least a portion of one ring.

Various systems, devices, and methods for endovascular implants and accurate placement thereof are disclosed. The implants include a proximal implant segment, a distal implant segment, connector struts connecting the proximal implant segment to the distal implant segment, and a side opening between the proximal implant segment and the distal implant segment. The implants can be used to create an arteriovenous fistula or connect one vessel of the body to another by placement of the proximal implant segment and the distal implant segment within the vessels to be connected. The implants can have an hourglass shape. The implants can include a continuous strut or ring at a distal edge of the proximal implant segment. Also disclosed are methods for accurate percutaneous placement of the implants disclosed, and a device for percutaneous delivery.

The peripheral vascular stent comprises scaffolding holding units and a membrane, each scaffolding holding units is formed of a closed ring shape wire; the membrane is covered on scaffolding holding units, the flexibility of the membrane is greater than that of the scaffolding holding units, between the wires of the same scaffolding holding unit and/or between two adjacent scaffolding holding units is provided a plurality of hollowed-out areas on the membrane, and two adjacent scaffolding holding units are only connected by the membrane beyond the hollowed-out areas. The peripheral vessel stent can meet the mechanical performance requirements, has a proper radial support force and good flexibility, and can well reduce the in-stent chronic external expansion force, has the advantages of little impact on blood flow, little injury to the vascular wall, and less likely to cause secondary thrombosis.

The invention includes modifications of a Z stent to allow the top struts of two Z stents deployed in the vena cava in a bilateral relationship, to interleave. One embodiment includes Z stents with angled top surfaces. A second embodiment includes Z stents having an intermediary suture but lacking the top suture in the topmost stent of a stacked stent module.

An apparatus may be used after a surgical procedure to protect against leaks and to separate healing tissue from foreign materials such as nutritional contents. In some cases the apparatus may be easily delivered to a surgical site before, during or after a surgical procedure such as gastric bypass surgery, but this is only an example. The apparatus may include expandable anchors at either end and a collapsible central portion extending between the two expandable anchors.

A delivery system for delivering and deploying stents with proximal and distal apices includes a guidewire catheter, a nose cone assembly, a proximal capture portion and a stent graft with proximal and distal stents. The nose cone assembly is at the distal end of the guidewire catheter and includes a nose cone and a distal capture portion. The proximal capture portion is proximal to the distal capture portion of the nose cone assembly. The proximal stent is releasably secured to the distal capture portion and the distal stent is releasably secured to the proximal capture portion. The stent graft can be deployed by releasing the proximal stent and the distal stent from proximal and distal capture portions of the delivery system.

The present disclosure relates generally to stents, systems, and methods for gastrointestinal treatment. In some embodiments, a stent may include a tubular scaffold having a first end opposite a second end, wherein a lumen extends between the first and second ends. The tubular scaffold may include a flared section and a medial section extending from the flared section, wherein a first diameter of the flared section is greater than a second diameter of the medial section. The stent may further include a liner extending partially along a surface of the tubular scaffold, wherein the liner is spaced from an anchoring region of the flared section to promote tissue ingrowth with the flared section.

The present invention provides a method for stabilizing a fractured bone. The method includes positioning an elongate rod in the medullary canal of the fractured bone and forming a passageway through the cortex of the bone. The passageway extends from the exterior surface of the bone to the medullary canal of the bone. The method also includes creating a bonding region on the elongate rod. The bonding region is generally aligned with the passageway of the cortex. Furthermore, the method includes positioning a fastener in the passageway of the cortex and on the bonding region of the elongate rod and thermally bonding the fastener to the bonding region of the elongate rod while the fastener is positioned in the passageway of the cortex.

A bioabsorbable composite stent structure, comprising bioabsorbable polymeric ring structures which retain a molecular weight and mechanical strength of a starting substrate and one or more interconnecting struts which extend between and couple adjacent ring structures. The ring structures can have a formed first diameter and being radially compressible to a smaller second diameter and re-expandable to the first diameter. The ring structures can comprise a base polymeric layer. The interconnecting struts can be formed from a polymer blend or co-polymer of poly-L-lactide (PLLA) and an elastomeric polymer. The interconnecting struts each can have a width that is less than a circumference of one of the ring structures. The adjacent ring structures can be axially and rotationally movable relative to one another via the interconnecting struts. The interconnecting struts can also be bioabsorbable.