FDA Device Intelligence
HomeDevice types › KXB

Prosthesis, Hip, Pelvifemoral Resurfacing, Metal/Polymer

FDA product code KXB · Class 3 · Orthopedic

0
Registered devices
1
Adverse events
3
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2023-05-30Synovo ProductionMedical device components were marketed without FDA clearance and without FDA approval
2023-05-30Synovo ProductionMedical device components were marketed without FDA clearance
2023-05-30Synovo ProductionMedical device components were marketed without FDA clearance

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