Product code
FWM: Prosthesis, breast, inflatable, internal, saline
FDA product code · Class III · General & Plastic Surgery
Key facts
| Product code | FWM |
|---|---|
| Device | Prosthesis, breast, inflatable, internal, saline |
| Device class | Class III |
| Regulation number | 878.3530 |
| Review panel | General & Plastic Surgery |
| Medical specialty | General & Plastic Surgery |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | Yes |
| Life-sustaining or life-supporting | No |
| Definition | Call for PMAs to be filed by 11/17/99 per 64 FR 45161 on 8/19/99 |
At a glance
- None 510(k) clearances
- None De Novo grants
- 1–9 PMA approvals
- None HDE approvals
- 100–999 UDI devices (GUDID)
- 1,000+ MAUDE adverse event reports
- 1–9 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database