Aortic stent grafts
Cook
A non-bioabsorbable tubular device intended to be implanted within the descending thoracic aorta to repair the vessel [includes repair of thoracic aortic aneurysm (TAA), traumatic transsections/dissections, fistulae, penetrating ulcers]; it is not intended for implantation within the aortic arch. It is typically made of a metal alloy [e.g., nickel-titanium alloy (Nitinol)] that forms an outer mesh structure with an inner synthetic polymer tube (endovascular graft) and is typically designed as a single continuous tube which may be used in singular and/or modular configurations. It is intended for percutaneous introduction; disposable delivery device (e.g., balloon catheter) may be included.
Cook 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 |
|---|---|---|---|
| G47436 | — | MR Conditional | Available |
| G47437 | — | MR Conditional | Available |
| G47438 | — | MR Conditional | Available |
| G47439 | — | MR Conditional | Available |
| G47440 | — | MR Conditional | Available |
| G47441 | — | MR Conditional | Available |
| G47442 | — | MR Conditional | Available |
| G47443 | — | MR Conditional | Available |
| G47444 | — | MR Conditional | Available |
| G47445 | — | MR Conditional | Available |
| G47446 | — | MR Conditional | Available |
| G47447 | — | MR Conditional | Available |
| G47448 | — | MR Conditional | Available |
| G47449 | — | MR Conditional | Available |
| G47450 | — | MR Conditional | Available |
| G47451 | — | MR Conditional | Available |
| G47452 | — | MR Conditional | Available |
| G47453 | — | MR Conditional | Available |
| G47454 | — | MR Conditional | Available |
| G47455 | — | MR Conditional | Available |
| G47456 | — | MR Conditional | Available |
| G47457 | — | MR Conditional | Available |
| G47458 | — | MR Conditional | Available |
| G47459 | — | MR Conditional | Available |
| G47460 | — | MR Conditional | Available |
| G47461 | — | MR Conditional | Available |
| G47462 | — | MR Conditional | Available |
| G47463 | — | MR Conditional | Available |
| G47464 | — | MR Conditional | Available |
| G47465 | — | MR Conditional | Available |
| G47466 | — | MR Conditional | Available |
| G47467 | — | MR Conditional | Available |
| G47468 | — | MR Conditional | Available |
| G47469 | — | MR Conditional | Available |
| G47470 | — | MR Conditional | Available |
| G47471 | — | MR Conditional | Available |
| G47472 | — | MR Conditional | Available |
| G47473 | — | MR Conditional | Available |
| G47474 | — | MR Conditional | Available |
| G47475 | — | MR Conditional | Available |
| G47476 | — | MR Conditional | Available |
| G47477 | — | MR Conditional | Available |
| G47478 | — | MR Conditional | Available |
| G47479 | — | MR Conditional | Available |
| G47480 | — | MR Conditional | Available |
| G47481 | — | MR Conditional | Available |
| G47482 | — | MR Conditional | Available |
| G47483 | — | MR Conditional | Available |
| G47484 | — | MR Conditional | Available |
| G47485 | — | MR Conditional | Available |
| G47486 | — | MR Conditional | Available |
| G47487 | — | MR Conditional | Available |
| G47488 | — | MR Conditional | Available |
| G47489 | — | MR Conditional | Available |
| G47491 | — | MR Conditional | Available |
| G47492 | — | MR Conditional | Available |
| G47493 | — | MR Conditional | Available |
| G47494 | — | MR Conditional | Available |
| G47495 | — | MR Conditional | Available |
| G47496 | — | MR Conditional | Available |
FDA clearances
- PMA P180001 July 2024
Procedures that use aortic stent grafts
Frequently asked questions
What is Cook used for?
A non-bioabsorbable tubular device intended to be implanted within the descending thoracic aorta to repair the vessel [includes repair of thoracic aortic aneurysm (TAA), traumatic transsections/dissections, fistulae, penetrating ulcers]; it is not intended for implantation within the aortic arch. It is typically made of a metal alloy [e.g., nickel-titanium alloy (Nitinol)] that forms an outer mesh structure with an inner synthetic polymer tube (endovascular graft) and is typically designed as a single continuous tube which may be used in singular and/or modular configurations. It is intended for percutaneous introduction; disposable delivery device (e.g., balloon catheter) may be included.
Who makes Cook?
Cook is made by William Cook Europe ApS. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Cook come in?
The FDA device database does not list sizes for Cook. Check the instructions for use or ask a William Cook Europe ApS representative.
Is Cook MRI safe?
The FDA device database lists Cook as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Cook FDA cleared?
Cook is covered by FDA submission P180001.
How do I contact a William Cook Europe ApS sales representative?
William Cook Europe ApS has not listed representatives on LA Vascular yet. Visit the William Cook Europe ApS 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.