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Knee Arthroplasty Implantation System

FDA product code OOG · Class 2 · Orthopedic

6,762
Registered devices
261
Adverse events
3
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-08-31ConforMIS, Inc.May contain small amounts of ethylene glycol residue
2015-08-31ConforMIS, Inc.May contain small amounts of ethylene glycol residue
2015-08-31ConforMIS, Inc.May contain small amounts of ethylene glycol residue

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