Medical Device Recalls
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1 result found
510(K) Number: K103655 |
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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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| Octane-C Cervical, 6® Lordotic Intended for anterior cervical spine intervertebral body fusion proc... | 2 | 07/31/2012 |
FEI # 1038671 Exactech, Inc. |
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