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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K130595
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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TIBIO FEM/FEM NAIL. 2 12/27/2013 Zimmer, Inc.
TIB NAIL 2 12/27/2013 Zimmer, Inc.
NGK Stem Ext 24 x 245mm 2 12/27/2013 Zimmer, Inc.
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