FDA product code MPJ: Interarticular Disc Prosthesis (Interpositional Implant)
MPJ is the FDA product code for interarticular disc prosthesis (interpositional implant). It is a Class III device, regulated under 21 CFR 872.3970 and reviewed by the Dental panel. Devices under MPJ reach the market by PMA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Interarticular Disc Prosthesis (Interpositional Implant) |
| Device class | Class III |
| Regulation | 21 CFR 872.3970 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | PMA |
| Implant | Yes |
Recalls for MPJ devices
openFDA lists no recalls for product code MPJ.
Frequently asked questions
What is FDA product code MPJ?
MPJ is the FDA product code for interarticular disc prosthesis (interpositional implant). It is a Class III device, regulated under 21 CFR 872.3970 and reviewed by the Dental panel.
What device class is MPJ?
Class III, regulation 21 CFR 872.3970. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MPJ
- Run a recall and safety report across every MPJ manufacturer
- Watch product code MPJ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.