A system for delivering an implant within a patient is disclosed. The activation of the heater coil causes the degradation, melting or reduction of a component that brings the heater coil into or out of electrical contact with another component, or causes the individual loops of the coil to contact each other, thereby resulting a notable change in resistance in the circuit supplying the heater coil with electricity. A core wire terminates prior to the distal end of the device, allowing for greater flexibility.

Data supported zero displacement implant/coil detachment system is, for example, gamma-irradiated post manufacturing, but made with no tension/zero displacement using more than 1 SR thread.

A device for occluding a vasculature of a patient including a micrograft having an absorbent polymeric structure with a lumen of transporting blood. The micrograft has a series of peaks and valleys formed by crimping. The occluding device is sufficiently small and flexible to be tracked on a guidewire and/or pushed through a microcatheter to a site within the vasculature of the patient. Delivery systems for delivering the micrografts are also disclosed.

A delivery member is provided for delivering and deploying an intravascular medical device. The delivery member includes a flexible distal portion including a wound wire coil surrounded by a flexible sleeve and inhibited from extending lengthwise by a stretch resistant member positioned through the lumen of the coil. The delivery member can include hypotubes positioned on either side (distally and proximally) from the wound wire coil to which the stretch resistant member and the wound wire coil can be attached.

Devices, systems, and methods for treating vascular defects are disclosed herein. One aspect of the present technology, for example, includes an occlusive device comprising a mesh having a low-profile state for intravascular delivery to the aneurysm and a deployed state, the mesh comprising a first end portion, a second end portion, and a length extending between the first and second end portions, and a first lateral edge, a second lateral edge, and a width extending between the first and second lateral edges. The mesh may have a predetermined shape in the deployed state in which (a) the mesh is curved along its width, (b) the mesh is curved along its length, and (c) the mesh has an undulating contour across at least a portion of one or both of its length or its width. The mesh is configured to be positioned within the aneurysm in the deployed state such that the mesh extends over the neck of the aneurysm.

An embolic coil conveying device and a preparation method thereof are disclosed. The embolic coil conveying device includes a pusher and an embolic coil. A distal end of the pusher and a proximal end of the embolic coil are connected to serve as a detachment section. A stretch-resistant thread is disposed in the embolic coil. The stretch-resistant thread is fixed at the proximal end of the embolic coil. A conductive wire is disposed in the pusher. The stretch-resistant thread is connected to the conductive wire. Compared with the prior art, the present invention has the advantages that the stretch-resistant thread is fixed at the proximal end of the embolic coil, so that the stretch-resistant thread is connected to the conductive wire, thereby reducing the length of the detachment section, making the detachment section more flexible, and avoiding kick-out of a microcatheter due to release of the embolic coil.

An embolic device for treating aneurysms or other vascular disorders may be more compliant than conventional devices, while still achieving desired porosity. In particular, the device may achieve the desired porosity only at discrete sections along the length of the device where such a porosity is required (e.g., sections that will block the neck of the aneurysm upon deployment). The remaining sections of the device can be configured to increase the device's compliance. For example, the remaining sections can be formed from less material than the sections with the desired porosity. In some instances, the sections with the desired porosity are formed from mesh-screen segments and the remaining sections are formed from coil segments. In some instances, the mesh-screen segments are configured to further enhance the device's compliance. For example, the mesh-screen segment can be formed from a layered structure that achieves greater compliance than conventional braided structures.

A delivery member is provided for delivering and deploying an implantable medical device. The delivery member includes a distal hypotube, a flexible tubular section, a proximal hypotube, a lumen extending through the distal hypotube, flexible tubular section, and proximal hypotube, a stretch resistant member, and a flexible sleeve. The stretch resistant tube can be positioned outside of the lumen, affixed to the proximal and distal hypotubes, and extending along at least a portion of an outer surface of the flexible tubular section. The flexible sleeve can comprise one or more stretch resistant fibers positioned within a wall of the flexible sleeve. The flexible sleeve can cover at least a majority of an outer surface of the flexible tubular section.

An embolic coil implant having a stretch resistant fiber therethrough and dual-functional engagement feature at its proximal end is provided. The stretch resistant fiber can be effective to limiting separation of windings of the embolic coil. The engagement feature can provide an attachment for securing the embolic coil to an engagement system of a delivery tube and for securing the stretch resistant fiber at the proximal end of the embolic coil. The engagement feature can have two engagement surfaces affixed to a proximal end of the embolic coil that are longitudinally offset from each other by a distance that is about half of a diameter of a wire of the embolic coil.

Devices for the occlusion of body cavities, such as the embolization of vascular aneurysms and the like, and methods for making and using such devices. The devices may be comprised of novel expansile materials, novel infrastructure design, or both. The devices provided are very flexible and enable deployment with reduced or no damage to bodily tissues, conduits, cavities, etceteras.