Aortic stent grafts
Talent Abdominal
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 P070027 August 2016
Procedures that use aortic stent grafts
Frequently asked questions
What is Talent Abdominal 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 Talent Abdominal?
Talent Abdominal is made by Medtronic, Inc.. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Talent Abdominal come in?
The FDA device database does not list sizes for Talent Abdominal. Check the instructions for use or ask a Medtronic, Inc. representative.
Is Talent Abdominal MRI safe?
The FDA device database lists Talent Abdominal as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Talent Abdominal FDA cleared?
Talent Abdominal is covered by FDA submission P070027.
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.