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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K984053
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Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventric... 2 08/17/2023 FEI # 3015531529
Medtronic Neurosurgery
Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914... 1 06/27/2014 FEI # 3015531529
Medtronic Neurosurgery
Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Cathe... 1 06/27/2014 FEI # 3015531529
Medtronic Neurosurgery
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, ... 1 06/27/2014 FEI # 3015531529
Medtronic Neurosurgery
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Catalog No. 46913... 1 06/27/2014 FEI # 3015531529
Medtronic Neurosurgery
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Cathe... 1 06/27/2014 FEI # 3015531529
Medtronic Neurosurgery
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