PMA supplement
P020036 S008: CORDIS S.M.A.R.T. NITINOL STENT SYSTEM & S.M.A.R.T. CONTROL NITINOL STENT SYSTEM
FDA PMA supplement · Special (Immediate Track) · Cordis US Corporation
Key facts
| Original PMA | P020036 |
|---|---|
| Supplement number | S008 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | CORDIS S.M.A.R.T. NITINOL STENT SYSTEM & S.M.A.R.T. CONTROL NITINOL STENT SYSTEM |
| Generic name | STENT, ILIAC |
| Applicant | Cordis US Corporation |
| Product code | NIO |
| Received date | Aug 24, 2007 |
| Decision date | Sep 20, 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: