Medical Device Recalls
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1 result found
510(K) Number: K072791 |
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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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| Oblique Posterior Atraumatic Lumbar (OPAL) System, Polymeric spinal fusion cage, non-sterile, OPAL S... | 2 | 04/14/2016 |
FEI # 3008812560 Synthes (USA) Products LLC |
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