Medical Device Recalls
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1 result found
510(K) Number: K083076 |
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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 | Medtronic Neurosurgery |
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