Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K013031 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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. |
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 Porous and Non-Porous Revision Stem Adapters, manufactured and distributed by Zi... | 2 | 02/15/2005 | Zimmer Austin, Inc |
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