Medical Device Recalls
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1 result found
510(K) Number: K103034 |
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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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Transforminal Lumbar Interbody Fusion (TLIF) PEEK Inserter used in the Genesys Spine Apache" Interbo... | 2 | 06/01/2012 | Genesys Orthopedic Systems, LLC |
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