Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K023528 |
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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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Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 0, TIB B/PL, for cemente... | 2 | 06/30/2009 | Zimmer Inc. |
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Left, Size 00, for cemented use onl... | 2 | 06/30/2009 | Zimmer Inc. |
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 0, TIB B/PL, for cement... | 2 | 06/30/2009 | Zimmer Inc. |
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 00, for cemented use on... | 2 | 06/30/2009 | Zimmer Inc. |
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 3, For cemented use onl... | 2 | 01/09/2009 | Zimmer Inc. |
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