Medical Device Recalls
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1 result found
510(K) Number: K124004 |
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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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P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN... | 2 | 09/30/2015 | Medtronic Navigation, Inc. |
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