Product code
PJK: Tissue adhesive for internal use
FDA product code · Class III · General & Plastic Surgery
Key facts
| Product code | PJK |
|---|---|
| Device | Tissue adhesive for internal use |
| Device class | Class III |
| Regulation number | 878.4010 |
| 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 | Approximation of tissue layers where subcutaneous dead space exists between the tissue planes in abdominoplasty. |
At a glance
- None 510(k) clearances
- None De Novo grants
- 1–9 PMA approvals
- None HDE approvals
- 1–9 UDI devices (GUDID)
- 10–99 MAUDE adverse event reports
- None 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