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Medial Knee Implanted Shock Absorber

FDA product code QVV · Class 2 · Orthopedic

13
Registered devices
15
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-12-02Moximed, Inc.Knee implant may fracture due to a supplier-related issue with one component that has nonconforming geometry at the distal end of the absorber component that ma

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