Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K132640 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2, Left Lateral Catalog Number: M57220... | 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. |
| ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US... | 2 | 10/21/2015 | ConforMIS, Inc. |
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