Medical Device Recalls
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1 result found
510(K) Number: K152304 |
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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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Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less... | 2 | 12/13/2018 | Howmedica Osteonics Corp. |
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