Aortic stent grafts
Vela Proximal Endograft System
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.
Vela Proximal Endograft System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| A22-22/C75 V | — | MR Conditional | Available |
| A22-22/C75-O20 V | — | MR Conditional | Available |
| A22-22/C95 V | — | MR Conditional | Available |
| A22-22/C95-O20 V | — | MR Conditional | Available |
| A25-25/C75 V | — | MR Conditional | Available |
| A25-25/C75-O20 V | — | MR Conditional | Available |
| A25-25/C95 V | — | MR Conditional | Available |
| A25-25/C95-O20 V | — | MR Conditional | Available |
| A28-28/C75 V | — | MR Conditional | Available |
| A28-28/C75-O20 V | — | MR Conditional | Available |
| A28-28/C95 V | — | MR Conditional | Available |
| A28-28/C95-O20 V | — | MR Conditional | Available |
| A31-31/C80 V | — | MR Conditional | Available |
| A31-31/C80-O20 V | — | MR Conditional | Available |
| A31-31/C100 V | — | MR Conditional | Available |
| A31-31/C100-O20 V | — | MR Conditional | Available |
| A34-34/C80 V | — | MR Conditional | Available |
| A34-34/C80-O20 V | — | MR Conditional | Available |
| A34-34/C100 V | — | MR Conditional | Available |
| A34-34/C100-O20 V | — | MR Conditional | Available |
FDA clearances
- PMA P040002 February 2014
Procedures that use aortic stent grafts
Frequently asked questions
What is Vela Proximal Endograft System 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 Vela Proximal Endograft System?
Vela Proximal Endograft System is made by Endologix LLC. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Vela Proximal Endograft System come in?
The FDA device database does not list sizes for Vela Proximal Endograft System. Check the instructions for use or ask a Endologix LLC representative.
Is Vela Proximal Endograft System MRI safe?
The FDA device database lists Vela Proximal Endograft System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Vela Proximal Endograft System FDA cleared?
Vela Proximal Endograft System is covered by FDA submission P040002.
How do I contact a Endologix LLC sales representative?
Endologix LLC has not listed representatives on LA Vascular yet. Visit the Endologix LLC 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.