Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K061211 |
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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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NCB® cancellous screw | 2 | 11/06/2012 | Zimmer, Inc. |
NCB® screw ® 4.0 self-tapping | 2 | 11/06/2012 | Zimmer, Inc. |
NCB®-PT lateral proximal 3 hole tibial plate | 2 | 11/06/2012 | Zimmer, Inc. |
NCB Proximal Lateral Tibia, "NCB-PT LAX PROX 3H TIBIA", Various Sizes, Item Nos. 0202261205 0202261... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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