Aortic stent grafts
Endurant IIs
A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.
FDA clearances
- PMA P100021 July 2014
Procedures that use aortic stent grafts
Frequently asked questions
What is Endurant IIs used for?
A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.
Who makes Endurant IIs?
Endurant IIs is made by Medtronic, Inc.. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Endurant IIs come in?
The FDA device database does not list sizes for Endurant IIs. Check the instructions for use or ask a Medtronic, Inc. representative.
Is Endurant IIs MRI safe?
The FDA device database lists Endurant IIs as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Endurant IIs FDA cleared?
Endurant IIs is covered by FDA submission P100021.
How do I contact a Medtronic, Inc. sales representative?
Medtronic, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.