Medical Device Recalls
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1 result found
510(K) Number: K112316 |
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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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ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Large, 12 degr... | 2 | 12/16/2014 | 4-Web Inc. |
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