PMA supplement
P120020 S024: Supera Peripheral Stent System
FDA PMA supplement · 30-Day Notice · Abbott Vascular (Idef Technologies Inc)
Key facts
| Original PMA | P120020 |
|---|---|
| Supplement number | S024 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Supera Peripheral Stent System |
| Generic name | STENT, SUPERFICIAL FEMORAL ARTERY |
| Applicant | Abbott Vascular (Idef Technologies Inc) |
| Product code | NIP |
| Received date | Sep 1, 2020 |
| Decision date | Sep 30, 2020 |
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: