PMA supplement
P000029 S050: DEFLUX INJECTABLE GEL
FDA PMA supplement · 135 Review Track For 30-Day Notice · Palette Life Sciences
Key facts
| Original PMA | P000029 |
|---|---|
| Supplement number | S050 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | DEFLUX INJECTABLE GEL |
| Generic name | AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE |
| Applicant | Palette Life Sciences |
| Product code | LNM |
| Received date | Sep 19, 2008 |
| Decision date | May 21, 2009 |
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: