Peripheral stents
Zilver 518
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Zilver 518 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 |
|---|---|---|---|
| G31350 | β | MR Conditional | Available |
| G31351 | β | MR Conditional | Available |
| G31352 | β | MR Conditional | Available |
| G31354 | β | MR Conditional | Available |
| G31437 | β | MR Conditional | Available |
| G31438 | β | MR Conditional | Available |
| G31439 | β | MR Conditional | Available |
| G31441 | β | MR Conditional | Available |
| G36047 | β | MR Conditional | Available |
| G36048 | β | MR Conditional | Available |
| G36259 | β | MR Conditional | Available |
| G36260 | β | MR Conditional | Available |
| G43769 | β | MR Conditional | Available |
| G43770 | β | MR Conditional | Available |
| G43771 | β | MR Conditional | Available |
| G43772 | β | MR Conditional | Available |
| G43773 | β | MR Conditional | Available |
| G43774 | β | MR Conditional | Available |
| G43775 | β | MR Conditional | Available |
| G43776 | β | MR Conditional | Available |
| G43777 | β | MR Conditional | Available |
| G43778 | β | MR Conditional | Available |
| G43779 | β | MR Conditional | Available |
| G43780 | β | MR Conditional | Available |
| G43781 | β | MR Conditional | Available |
| G43782 | β | MR Conditional | Available |
| G43783 | β | MR Conditional | Available |
| G43784 | β | MR Conditional | Available |
| G43785 | β | MR Conditional | Available |
| G43786 | β | MR Conditional | Available |
| G43787 | β | MR Conditional | Available |
| G43788 | β | MR Conditional | Available |
| G43789 | β | MR Conditional | Available |
| G43790 | β | MR Conditional | Available |
| G43791 | β | MR Conditional | Available |
| G43792 | β | MR Conditional | Available |
| G43793 | β | MR Conditional | Available |
| G49309 | β | MR Conditional | Available |
| G49310 | β | MR Conditional | Available |
| G49311 | β | MR Conditional | Available |
| G49312 | β | MR Conditional | Available |
| G49313 | β | MR Conditional | Available |
| G49314 | β | MR Conditional | Available |
| G49315 | β | MR Conditional | Available |
| G49316 | β | MR Conditional | Available |
| G49317 | β | MR Conditional | Available |
| G49318 | β | MR Conditional | Available |
| G49319 | β | MR Conditional | Available |
| G49320 | β | MR Conditional | Available |
| G49321 | β | MR Conditional | Available |
| G49322 | β | MR Conditional | Available |
| G49323 | β | MR Conditional | Available |
| G49324 | β | MR Conditional | Available |
| G49325 | β | MR Conditional | Available |
| G49326 | β | MR Conditional | Available |
| G49327 | β | MR Conditional | Available |
| G49328 | β | MR Conditional | Available |
| G49329 | β | MR Conditional | Available |
| G49330 | β | MR Conditional | Available |
| G49331 | β | MR Conditional | Available |
| G49332 | β | MR Conditional | Available |
| G49333 | β | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is Zilver 518 used for?
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Who makes Zilver 518?
Zilver 518 is made by Cook Ireland Ltd. It is listed under peripheral artery stents and covered stents, biliary drainage catheters in our device library.
What sizes does Zilver 518 come in?
The FDA device database does not list sizes for Zilver 518. Check the instructions for use or ask a Cook Ireland Ltd representative.
Is Zilver 518 MRI safe?
The FDA device database lists Zilver 518 as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Zilver 518 FDA cleared?
Zilver 518 is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Cook Ireland Ltd sales representative?
Cook Ireland Ltd has not listed representatives on LA Vascular yet. Visit the Cook Ireland Ltd 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.