Medical Device Recalls
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1 result found
510(K) Number: K032064 |
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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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Theken L"POD" Titanium Vertebral Body Replacement System, Vu c"POD" PEEK-Optima® Vertebral Body Repl... | 2 | 05/19/2011 | Integra LifeSciences Corp. |
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