Peripheral stents

Zilver 518

by Cook Ireland Ltd

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.

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Zilver 518 models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
G31350β€” MR ConditionalAvailable
G31351β€” MR ConditionalAvailable
G31352β€” MR ConditionalAvailable
G31354β€” MR ConditionalAvailable
G31437β€” MR ConditionalAvailable
G31438β€” MR ConditionalAvailable
G31439β€” MR ConditionalAvailable
G31441β€” MR ConditionalAvailable
G36047β€” MR ConditionalAvailable
G36048β€” MR ConditionalAvailable
G36259β€” MR ConditionalAvailable
G36260β€” MR ConditionalAvailable
G43769β€” MR ConditionalAvailable
G43770β€” MR ConditionalAvailable
G43771β€” MR ConditionalAvailable
G43772β€” MR ConditionalAvailable
G43773β€” MR ConditionalAvailable
G43774β€” MR ConditionalAvailable
G43775β€” MR ConditionalAvailable
G43776β€” MR ConditionalAvailable
G43777β€” MR ConditionalAvailable
G43778β€” MR ConditionalAvailable
G43779β€” MR ConditionalAvailable
G43780β€” MR ConditionalAvailable
G43781β€” MR ConditionalAvailable
G43782β€” MR ConditionalAvailable
G43783β€” MR ConditionalAvailable
G43784β€” MR ConditionalAvailable
G43785β€” MR ConditionalAvailable
G43786β€” MR ConditionalAvailable
G43787β€” MR ConditionalAvailable
G43788β€” MR ConditionalAvailable
G43789β€” MR ConditionalAvailable
G43790β€” MR ConditionalAvailable
G43791β€” MR ConditionalAvailable
G43792β€” MR ConditionalAvailable
G43793β€” MR ConditionalAvailable
G49309β€” MR ConditionalAvailable
G49310β€” MR ConditionalAvailable
G49311β€” MR ConditionalAvailable
G49312β€” MR ConditionalAvailable
G49313β€” MR ConditionalAvailable
G49314β€” MR ConditionalAvailable
G49315β€” MR ConditionalAvailable
G49316β€” MR ConditionalAvailable
G49317β€” MR ConditionalAvailable
G49318β€” MR ConditionalAvailable
G49319β€” MR ConditionalAvailable
G49320β€” MR ConditionalAvailable
G49321β€” MR ConditionalAvailable
G49322β€” MR ConditionalAvailable
G49323β€” MR ConditionalAvailable
G49324β€” MR ConditionalAvailable
G49325β€” MR ConditionalAvailable
G49326β€” MR ConditionalAvailable
G49327β€” MR ConditionalAvailable
G49328β€” MR ConditionalAvailable
G49329β€” MR ConditionalAvailable
G49330β€” MR ConditionalAvailable
G49331β€” MR ConditionalAvailable
G49332β€” MR ConditionalAvailable
G49333β€” MR ConditionalAvailable

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.

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