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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K133256
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FDA Recall
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ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2, Left Lateral Catalog Number: M57220... 2 10/21/2015 ConforMIS, Inc.
ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US... 2 10/21/2015 ConforMIS, Inc.
ConFormis iDUO G2, Right Lateral Catalog Number: M5723INT0600240 (US) ... 2 10/21/2015 ConforMIS, Inc.
ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2, Left Lateral Catalog Number: M5723... 2 10/21/2015 ConforMIS, Inc.
ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number... 2 10/21/2015 ConforMIS, Inc.
ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220... 2 10/21/2015 ConforMIS, Inc.
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