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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 15 of 15 Results
510(K) Number: K072858
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Product Description
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FDA Recall
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TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 4 RIGHT, STERILE R, REF 12 000 024, S&N ... 2 04/21/2016 Smith & Nephew, Inc.
TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 6 RIGHT, STERILE R, REF 12 000 025, S&N ... 2 04/21/2016 Smith & Nephew, Inc.
TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 8 RIGHT, STERILE R, REF 12 000 026, S&N ... 2 04/21/2016 Smith & Nephew, Inc.
TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 10 RIGHT, STERILE R, REF 12 000 027, S&N... 2 04/21/2016 Smith & Nephew, Inc.
TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 8 LEFT, STERILE R, REF 12 000 005, S&N 75... 2 04/21/2016 Smith & Nephew, Inc.
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