Medical Device Recalls
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1 result found
510(K) Number: K031438 |
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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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Intramedullary Fixation Rod, common name Fibula Rod, labeled IM Rod System Manufactured or Distribu... | 2 | 05/10/2010 | Acumed LLC |
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