PMA supplement
P990004 S047: SURGIFOAM® Absorbable Gelatin Sponge, U.S.P., Hemorrhoidectomy Sponge/Oral Sponge and SURGIFOAM® Absorbable Gelatin Powd
FDA PMA supplement · 30-Day Notice · Ferrosan Meidcal Devices A/S
Key facts
| Original PMA | P990004 |
|---|---|
| Supplement number | S047 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | SURGIFOAM® Absorbable Gelatin Sponge, U.S.P., Hemorrhoidectomy Sponge/Oral Sponge and SURGIFOAM® Absorbable Gelatin Powd |
| Generic name | Agent, absorbable hemostatic, collagen based |
| Applicant | Ferrosan Meidcal Devices A/S |
| Product code | LMF |
| Received date | Apr 2, 2021 |
| Decision date | Apr 30, 2021 |
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: