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Knee Arthroplasty Implantation System
FDA product code OOG · Class 2 · Orthopedic
0
Registered devices
260
Adverse events
3
Recalls
2
510(k) clearances
Devices with this code
PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.EXULT Knee Replacement System — Corentec Co., LtdPROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY® — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.My Knee Tibial Cutting Blocks — Medacta International SAiTotal Identity CR — Conformis, Inc.PROPHECY® — Microport Orthopedics Inc.Signature — Materialise NVPointCloud Knee Instruments — Unik Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY® — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.Identity Imprint Knee Replacement System — Conformis, Inc.Identity Imprint Knee Replacement System — Conformis, Inc.My Knee Femoral Cutting Blocks MIS — Medacta International SAIdentity Imprint Porous CR — Conformis, Inc.PROPHECY — Microport Orthopedics Inc.iTotal Identity CR — Conformis, Inc.PROPHECY — Microport Orthopedics Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
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