PMA supplement
P150003 S105: SYNERGY XD Everolimus Eluting Platinum Chromium Coronary Stent System, SYNERGY SHIELD Everolimus Eluting Platinum Chromi
FDA PMA supplement · Panel Track · Boston Scientific Corporation
Key facts
| Original PMA | P150003 |
|---|---|
| Supplement number | S105 |
| Supplement type | Panel Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | SYNERGY XD Everolimus Eluting Platinum Chromium Coronary Stent System, SYNERGY SHIELD Everolimus Eluting Platinum Chromi |
| Generic name | Coronary drug-eluting stent |
| Applicant | Boston Scientific Corporation |
| Product code | NIQ |
| Received date | Jul 31, 2024 |
| Decision date | Jan 27, 2025 |
| Docket number | 25M-0347 |
At a glance
- No Expedited review granted
- Yes Approval order on file
- Yes 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: