Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K062029 |
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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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Anatomical Shoulder" Fracture Humeral stem | 2 | 11/06/2012 | Zimmer, Inc. |
Anatomical Shoulder" Fracture Humeral Head | 2 | 11/06/2012 | Zimmer, Inc. |
Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder Fracture Humeral stem ... | 2 | 11/06/2012 | Zimmer, Inc. |
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