Aortic stent grafts
Zenith Spiral-Z
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.
Procedures that use aortic stent grafts
Frequently asked questions
What is Zenith Spiral-Z 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 Zenith Spiral-Z?
Zenith Spiral-Z is made by Cook Incorporated. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Zenith Spiral-Z come in?
The FDA device database does not list sizes for Zenith Spiral-Z. Check the instructions for use or ask a Cook Incorporated representative.
Is Zenith Spiral-Z MRI safe?
The FDA device database lists Zenith Spiral-Z as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Zenith Spiral-Z FDA cleared?
Zenith Spiral-Z is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Cook Incorporated sales representative?
Cook Incorporated has not listed representatives on LA Vascular yet. Visit the Cook Incorporated 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.