A stent includes a tubular body possessing a plurality of gaps. The tubular body includes a plurality of circumferentially extending linear struts. The stent includes a plurality of links connecting the linear struts. At least one of the links has first and second connection portions. The first connection portion is integrally formed with one strut, and the second connection portion is integrally formed with an adjacent strut. The stent includes a biodegradable material between the first connection portion and the second connection portion to connect the first and second connection portions to each other. The biodegradable material restrains the one strut and the adjacent strut from moving to their original shapes. The first and second connection portions move relative to one another in a separation direction when a connection by the biodegradable material is released so that the original shapes of the struts are restored.

A system for reshaping a valve annulus includes an elongate template having a length along a longitudinal axis and at least one concavity in a generally lateral direction along said length. The pre-shaped template is positioned against at least a region of an inner peripheral wall of the valve annulus, and at least one anchor on the template is advanced into a lateral wall of the valve annulus to reposition at least one segment of the region of the inner peripheral wall of the valve annulus into said concavity. In this way, a peripheral length of the valve annulus can be foreshortened and/or reshaped to improve coaption of the valve leaflets and/or to eliminate or decrease regurgitation of a valve.

Methods for securing strand ends of devices configured for insertion into an anatomical structure, and the resulting devices.

A stent (scaffold) or other luminal prosthesis comprising circumferential structural elements which provide high strength after deployment and allows for scaffold to uncage, and/or allow for scaffold or luminal expansion thereafter. The circumferential scaffold is typically formed from non-degradable material and will be modified to expand and/or uncage after deployment.

Stent assemblies and related methods for creating an anastomosis employ a bioresorbable stent. A stent assembly includes a bioresorbable stent and one or more bioresorbable retention devices. The stent is configured for retaining a first section of a tubular organ in contact with a second section of the tubular organ to accommodate wound healing for connecting of the first and second sections of the tubular organ. A first end portion of the stent is configured to accommodate insertion into the first section of the tubular organ and inhibit removal from the first section of the tubular organ. A second end portion of the stent is configured to accommodate insertion into the second section of the tubular organ and inhibit removal from the second section of the tubular organ. The one or more retention devices are configurable to secure the first and second sections of the tubular organ to the stent.

An intraluminal support structure having a delivery configuration that is a crimped open configuration to increase flexibility while maneuvering in the anatomy and having a small scarring signature.

A system for reshaping a valve annulus includes an elongate template having a length along a longitudinal axis and at least one concavity in a generally lateral direction along said length. The pre-shaped template is positioned against at least a region of an inner peripheral wall of the valve annulus, and at least one anchor on the template is advanced into a lateral wall of the valve annulus to reposition at least one segment of the region of the inner peripheral wall of the valve annulus into said concavity. In this way, a peripheral length of the valve annulus can be foreshortened and/or reshaped to improve coaption of the valve leaflets and/or to eliminate or decrease regurgitation of a valve.

A stent retractor has a radially flexibly expandable tubular sheath divided in the peripheral direction into at least two sections, specifically a reinforcing section and an expanding section, with radial flexibilities that differ from one another, these sections being interconnected integrally. The stent retractor includes axial segments that are connected by a puzzle-type connection allowing simple separation or length adjustment in the axial direction (including when in situ) while also being made integrally, for example by a laser or water jet cutting method, preferably from a tubular blank.

Methods for securing strand ends of devices configured for insertion into an anatomical structure, and the resulting devices.

Various examples address support structures (e.g., prosthetic valve support structures or frames) that incorporate a frame that, upon transitioning to a deployed configuration, include a proximal section has increased stiffness, or resistance to deformation in a transverse plane to a longitudinal axis of a device, including resistance to a change in shape, size, or both. Such an increase in transverse deformation resistance may be measured as an increase in radial compressive resistance or an increase in flat plate stiffness, for example, or both. Such increases in transverse deformation resistance may be realized through a reduction in length of the increased stiffness region of the support structure, such as through longitudinal compression of the region following an initial radial expansion of the region.