PMA supplement
P880003 S054: CORDIS PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY DILATATION CATHETERS
FDA PMA supplement · Normal 180 Day Track · Cordis Corp.
Key facts
| Original PMA | P880003 |
|---|---|
| Supplement number | S054 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | CORDIS PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY DILATATION CATHETERS |
| Generic name | Catheters, transluminal coronary angioplasty, percutaneous |
| Applicant | Cordis Corp. |
| Product code | LOX |
| Received date | Dec 12, 1995 |
| Decision date | Jun 13, 1996 |
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: