FDA product code JDD: Prosthesis, Upper Femoral
JDD is the FDA product code for prosthesis, upper femoral. It is a Class II device, regulated under 21 CFR 888.3360 and reviewed by the Orthopedic panel. Devices under JDD reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Prosthesis, Upper Femoral |
| Device class | Class II |
| Regulation | 21 CFR 888.3360 |
| Review panel | OR — Orthopedic |
| Medical specialty | Orthopedic |
| Premarket route | 510(k) |
| Implant | Yes |
Recalls for JDD devices
openFDA lists no recalls for product code JDD.
Frequently asked questions
What is FDA product code JDD?
JDD is the FDA product code for prosthesis, upper femoral. It is a Class II device, regulated under 21 CFR 888.3360 and reviewed by the Orthopedic panel.
What device class is JDD?
Class II, regulation 21 CFR 888.3360. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code JDD
- Run a recall and safety report across every JDD manufacturer
- Watch product code JDD 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.
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