Medical Device Recalls
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1 result found
510(K) Number: K060681 |
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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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| Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for th... | 2 | 02/12/2021 |
FEI # 3015531529 Medtronic Neurosurgery |
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