PMA supplement
P020023 S005: RESTYLANE INJECTABLE GEL
FDA PMA supplement · 30-Day Notice · Q-Med AB
Key facts
| Original PMA | P020023 |
|---|---|
| Supplement number | S005 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | RESTYLANE INJECTABLE GEL |
| Generic name | Implant, dermal, for aesthetic use |
| Applicant | Q-Med AB |
| Product code | LMH |
| Received date | Apr 15, 2004 |
| Decision date | May 10, 2004 |
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: