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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 16 Results
510(K) Number: K090596
 
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Product Description
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FDA Recall
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Zimmer Natural Nail System, Tibial Targeting Guide Handle, tall, nonsterile, Zimmer, Warsaw, IN; REF... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Tibial Targeting Guide Handle, small, nonsterile, Zimmer, Warsaw, IN; RE... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Tibial Module, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-005-04. Th... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Connecting Knob, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-000-11. ... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral interlock Module, tall, nonsterile, Zimmer, Warsaw, IN... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, tall, nonsterile, Zimmer, Wars... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, standard, nonsterile, Zimmer, ... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, standard, 0.512" wide, nonster... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, small, nonsterile, Zimmer, War... 2 11/24/2009 Zimmer Inc.
Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, small, 0.512" wide, nonsterile... 2 11/24/2009 Zimmer Inc.
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