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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: K935523
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Recall
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FDA Recall
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Recalling Firm
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Natural-Knee®/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1 NATURAL-KNEE M/B PAT SZ2 NATURAL... 2 03/20/2014 Zimmer, Inc.
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