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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K011138
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Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UNLESS PACK ... 2 06/29/2011 FEI # 3002806535
Biomet U.K., Ltd.
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