PMA supplement
P020026 S042: CORDIS CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA PMA supplement · Normal 180 Day Track No User Fee · Cordis Corp.
Key facts
| Original PMA | P020026 |
|---|---|
| Supplement number | S042 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | CORDIS CYPHER SIROLIMUS-ELUTING CORONARY STENT |
| Generic name | Coronary drug-eluting stent |
| Applicant | Cordis Corp. |
| Product code | NIQ |
| Received date | Sep 6, 2007 |
| Decision date | Oct 16, 2007 |
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: