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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K013031
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Product Description
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FDA Recall
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MOST Options System Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zi... 2 02/15/2005 Zimmer Austin, Inc
Zimmer Most Hinged Tibia Baseplate Spacer, size 1, 6 mm, sterile, Zimmer, Warsaw, IN; REF 5020-06-00... 2 03/09/2009 Zimmer Inc.
MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM HINGED TIB INS SZ 4 6MM M HINGED TIB INS SZ ... 2 03/20/2014 Zimmer, Inc.