PMA supplement
P080007 S026: E-Luminexx® Vascular Stent
FDA PMA supplement · Real-Time Process · Bard Peripheral Vascular, Inc.
Key facts
| Original PMA | P080007 |
|---|---|
| Supplement number | S026 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | E-Luminexx® Vascular Stent |
| Generic name | STENT, ILIAC |
| Applicant | Bard Peripheral Vascular, Inc. |
| Product code | NIO |
| Received date | Aug 26, 2021 |
| Decision date | Nov 23, 2021 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: