Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 03/06/2015 510(K) Number: K073347 |
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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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Dynesys® Top-Loading System Cannulated Pedicle + Set Screw | 2 | 11/06/2012 | Zimmer, Inc. |
Zimmer Dynesys top-loading cutter, spacer, Zimmer Spine, Minneapolis, MN; REF 07.01284.001. | 2 | 11/19/2009 | Zimmer Inc. |
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