Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K093513 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2, Left Lateral Catalog Number: M5723... | 2 | 10/21/2015 | ConforMIS, Inc. |
ConFormis iDUO G2, Right Lateral Catalog Number: M5723INT0600240 (US) ... | 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. |
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