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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K142404
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Product Description
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FDA Recall
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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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