Medical Device Recalls
-
11 to 16 of 16 Results
510(K) Number: K090596 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Zimmer Natural Nail System, Antegrade Femoral Interlock Module, small, nonsterile, Zimmer, Warsaw, I... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Antegrade Femoral Recon Module, small, nonsterile, Zimmer, Warsaw, IN; R... | 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, 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, small, nonsterile, Zimmer, War... | 2 | 11/24/2009 | Zimmer Inc. |
-