Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142404 |
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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 iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT a... | 2 | 10/21/2015 | ConforMIS, Inc. |
ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2, Right Medial Catalog Number:M57220600... | 2 | 10/21/2015 | ConforMIS, Inc. |
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