FDA Device Intelligence
HomeDevice types › KRP

Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Metal

FDA product code KRP · Class 3 · Orthopedic

0
Registered devices
62
Adverse events
1
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2004-08-20Philips Medical Systems Sales & Service Region No. AmericaPotential for patient burn

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.