Peripheral stents
Zilver PTX
A non-bioabsorbable metal tubular mesh structure with a drug coating intended to be implanted into a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to maintain luminal patency typically in patients with symptomatic peripheral artery disease; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. The drug coating is slowly released and intended to inhibit restenosis. Disposable devices associated with implantation (e.g., delivery catheter) may be included.
Zilver PTX 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 |
|---|---|---|---|
| G24888 | — | MR Conditional | Available |
| G24889 | — | MR Conditional | Available |
| G24890 | — | MR Conditional | Available |
| G24891 | — | MR Conditional | Available |
| G24894 | — | MR Conditional | Available |
| G24895 | — | MR Conditional | Available |
| G24896 | — | MR Conditional | Available |
| G24914 | — | MR Conditional | Available |
| G24916 | — | MR Conditional | Available |
| G24935 | — | MR Conditional | Available |
| G24937 | — | MR Conditional | Available |
| G24939 | — | MR Conditional | Available |
| G34313 | — | MR Conditional | Available |
| G34314 | — | MR Conditional | Available |
| G38404 | — | MR Conditional | Available |
| G38407 | — | MR Conditional | Available |
| G38408 | — | MR Conditional | Available |
| G38414 | — | MR Conditional | Available |
| G38415 | — | MR Conditional | Available |
| G38416 | — | MR Conditional | Available |
| G38463 | — | MR Conditional | Available |
| G38479 | — | MR Conditional | Available |
| G38480 | — | MR Conditional | Available |
| G38481 | — | MR Conditional | Available |
| G38482 | — | MR Conditional | Available |
| G38483 | — | MR Conditional | Available |
| G38486 | — | MR Conditional | Available |
| G38487 | — | MR Conditional | Available |
| G38488 | — | MR Conditional | Available |
| G38489 | — | MR Conditional | Available |
| G38490 | — | MR Conditional | Available |
| G38491 | — | MR Conditional | Available |
| G38495 | — | MR Conditional | Available |
| G38516 | — | MR Conditional | Available |
| G38518 | — | MR Conditional | Available |
| G38523 | — | MR Conditional | Available |
| G38532 | — | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is Zilver PTX used for?
A non-bioabsorbable metal tubular mesh structure with a drug coating intended to be implanted into a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to maintain luminal patency typically in patients with symptomatic peripheral artery disease; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. The drug coating is slowly released and intended to inhibit restenosis. Disposable devices associated with implantation (e.g., delivery catheter) may be included.
Who makes Zilver PTX?
Zilver PTX is made by Cook Ireland Ltd. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does Zilver PTX come in?
The FDA device database does not list sizes for Zilver PTX. Check the instructions for use or ask a Cook Ireland Ltd representative.
Is Zilver PTX MRI safe?
The FDA device database lists Zilver PTX as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Zilver PTX FDA cleared?
Zilver PTX 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.