FDA Device Intelligence
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Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented

FDA product code OQG · Class 2 · Orthopedic

5,737
Registered devices
673
Adverse events
2
Recalls
20
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-06-16Conformis, Inc.30mm screws were labeled as 25mm screws.
2013-01-24Stelkast CoFirm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell.

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