Medical Device Recalls
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1 result found
510(K) Number: K110733 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical C... | 2 | 08/27/2013 |
FEI # 3006755626 SpineNet |
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