Medical Device Recalls
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1 result found
510(K) Number: K030710 |
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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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Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic Implant) Product Usage: ... | 2 | 12/05/2012 | Biomet, Inc. |
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