FDA product code LPF: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic, Cemented
LPF is the FDA product code for prosthesis, hip, semi-constrained, metal/ceramic/ceramic, cemented. It is a Class III device, reviewed by the Orthopedic panel. Devices under LPF reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic, Cemented |
| Device class | Class III |
| Review panel | OR — Orthopedic |
| Medical specialty | Unknown |
| Premarket route | PMA |
| Implant | Yes |
Recalls for LPF devices
openFDA lists no recalls for product code LPF.
Frequently asked questions
What is FDA product code LPF?
LPF is the FDA product code for prosthesis, hip, semi-constrained, metal/ceramic/ceramic, cemented. It is a Class III device, reviewed by the Orthopedic panel.
What device class is LPF?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code LPF
- Run a recall and safety report across every LPF manufacturer
- Watch product code LPF 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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