| Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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| Device | Venovo™ Venous Stent System |
| Generic Name | Stent, iliac vein |
| Applicant | Bard Peripheral Vascular, Inc. 1625 W Third St. Tempe, AZ 85281 |
| PMA Number | P180037 |
| Supplement Number | S015 |
| Date Received | 05/22/2026 |
| Decision Date | 06/10/2026 |
| Product Code |
QAN |
| Advisory Committee |
Cardiovascular |
| Supplement Type | 30-Day Notice |
| Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement changes to the packaging supplier's adhesive coating |
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