PMA supplement
P880003 S083: RAPTORAIL PTCA DILATATION CATHETER (RX)
FDA PMA supplement · Special (Immediate Track) · Cordis Corp.
Key facts
| Original PMA | P880003 |
|---|---|
| Supplement number | S083 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | RAPTORAIL PTCA DILATATION CATHETER (RX) |
| Generic name | Catheters, transluminal coronary angioplasty, percutaneous |
| Applicant | Cordis Corp. |
| Product code | LOX |
| Received date | Feb 1, 2002 |
| Decision date | Feb 12, 2002 |
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: