Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K063432 |
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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 iUni ( Unicondylar Knee System ) Left Medial Implant Kit Product Code: M57220600010. ... | 2 | 07/15/2009 | Conformis Inc |
ConforMIS iUni ( Unicondylar Knee System iUni Right Lateral Implant Kit Product Code: M57220600040. ... | 2 | 07/15/2009 | Conformis Inc |
ConforMIS iUni ( Unicondylar Knee System ) iUni Right Medial Implant Kit Product Code : M5722060002... | 2 | 07/15/2009 | Conformis Inc |
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