PMA supplement
P160025 S018: Pulsar-18 T3 Stent System
FDA PMA supplement · Special (Immediate Track) · Biotronik AG
Key facts
| Original PMA | P160025 |
|---|---|
| Supplement number | S018 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Pulsar-18 T3 Stent System |
| Generic name | STENT, SUPERFICIAL FEMORAL ARTERY |
| Applicant | Biotronik AG |
| Product code | NIP |
| Received date | Dec 10, 2024 |
| Decision date | Dec 11, 2024 |
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: