Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2103-2013 - SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in skeletally mature patients with degenerative disc di... | 2 | 08/27/2013 |
FEI # 3006755626 SpineNet |
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