An embolic coil is formed by being spirally wound by an element wire and is filled into an aneurysm. The embolic coil includes: a first coil portion, in which a large-diameter coil portion wound to have a large diameter D1 and a small-diameter coil portion wound to have a diameter D2 smaller than the large-diameter coil portion are arranged in a plurality of coils and alternately in a longitudinal direction Y of the embolic coil. A second coil portion is wound to be continuous with the first coil portion and to have a surface flatter than the first coil portion.

A fallopian biocompatible plug can include differently expandable portions. A method of treating a uterine abnormality of a patient includes: providing an endoscope having a working channel; inflating a uterine cavity with a fluid; delivering a biocompatible plug into an ostium of a fallopian tube of the patient, wherein the biocompatible plug is substantially cylindrical in form and configured to be radially expandable, wherein the biocompatible plug is configured to expand in the ostium of the fallopian tube to seal the fallopian tube from the uterine cavity; delivering a resection device through the working channel; and resecting the uterine abnormality.

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. The distal hypotube can include attachment slots for positioning and attaching a loop wire to the distal hypotube.

An intrasacular aneurysm occlusion device can be a peanut, hourglass, and/or hyperbolic shaped mesh which is inserted and expanded within an aneurysm sac. The proximal lobe of the device reduces blood flow into the sac through the aneurysm neck and the distal lobe of the device contacts the dome of the sac so as to keep the proximal lobe from shifting. The narrow center portion of the peanut, hourglass, or hyperbolic mesh can bend so that the device at least partially conforms to the interior of an irregularly-shaped aneurysm sac.

This intrasacular aneurysm occlusion device includes a neck bridge with a closeable opening through which embolic material is inserted into an aneurysm sac. After the neck bridge has been expanded within the aneurysm sac, a catheter is inserted through the opening and embolic material is delivered through the catheter into the aneurysm sac. After the aneurysm sac has been filled with embolic material, the catheter is then withdrawn and the opening is closed so that embolic material does not escape out of the aneurysm sac.

This application describes various embodiments of an expandable device that includes at least one support member. The support member (or members) is integrated into the structure of the expandable device and increases its column strength, which thus augments pushability of the expanding device through a delivery catheter. The support member allows force applied while pushing from the proximal end of the expandable device to be translated to the distal end of the device and therefore avoid bunching or deformation without increasing the profile of the device to a degree that would prohibit passage through a lumen of a specific required size. Thus, the expandable devices described herein address at least some of the shortcomings discussed above.

Apparatus, systems, and methods are provided for monitoring AF episodes, delivering ATP pulses, and/or achieving electrical isolation of the left atrial appendage (LAA) of a patient's heart and/or preventing thrombus formation after electrical isolation. For example, devices are provided that may implanted from within the left atrium, e.g., to isolate the LAA, prevent thrombus formation within the LAA, facilitate endothelialization, and/or deliver pacing.

Devices and methods for treatment of a patient's vasculature are described. Embodiments may include a device that includes a plurality of permeable shells connected by a plurality of coils, each coil connecting at least one pair of permeable shells. The plurality of coils may include an inert hydrogel core that absorbs water.

Non-expandable space-occupying devices for treating voids within the body are disclosed. The devices can have multiple non-expandable space-occupying elements connected to a flexible leader. Methods of making and using the devices are also disclosed.

An embodiment of the invention includes an expandable implant to endovascularly embolize an anatomical void or malformation, such as an aneurysm. An embodiment is comprised of a chain or linked sequence of expandable polymer foam elements. Another embodiment includes an elongated length of expandable polymer foam coupled to a backbone. Another embodiment includes a system for endovascular delivery of an expandable implant (e.g., shape memory polymer) to embolize an aneurysm. The system may include a microcatheter, a lumen-reducing collar coupled to the distal tip of the microcatheter, a flexible pushing element detachably coupled to an expandable implant, and a flexible tubular sheath inside of which the compressed implant and pushing element are pre-loaded. Other embodiments are described herein.