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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: K972501
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Recall
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FDA Recall
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Apollo" Revision/Constrained Knee System: SZ0-16MM AK CCK TIB INSER SZ1-11MM AK CCK TIB INSER SZ1... 2 03/20/2014 Zimmer, Inc.
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