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SENZA Adverse Event — Injury (MDR 3008514029-2020-00533)

SENZA Adverse Event — Injury (MDR 3008514029-2020-00533) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SENZA; Generic name: NEVRO SENZA; Manufacturer: NEVRO CORP..

DeviceSENZA
Generic nameNEVRO SENZA
ManufacturerNEVRO CORP.
Report number3008514029-2020-00533
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE
NarrativeTHE MANUFACTURING RECORDS WERE REVIEWED AND NO ISSUES WERE FOUND RELATED TO THE NATURE OF THE COMPLAINT. THE DEVICE WAS NOT RETURNED.
SourceopenFDA MAUDE (device adverse events)

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