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PRECICE BONE TRANSPORT SYSTEM Adverse Event — Malfunction (MDR 3006179046-2020-00293)

PRECICE BONE TRANSPORT SYSTEM Adverse Event — Malfunction (MDR 3006179046-2020-00293) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECICE BONE TRANSPORT SYSTEM; Generic name: FIXATION DEVICE, INTERNAL, NAIL, INTRAMEDULLARY; Manufacturer: NUVASIVE SPECIALIZED ORTHOPEDICS, INC

DevicePRECICE BONE TRANSPORT SYSTEM
Generic nameFIXATION DEVICE, INTERNAL, NAIL, INTRAMEDULLARY
ManufacturerNUVASIVE SPECIALIZED ORTHOPEDICS, INCORPORATED
Report number3006179046-2020-00293
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeB.5: SEE UPDATED INFORMATION IN H2, H3, H6 AND H10.
SourceopenFDA MAUDE (device adverse events)

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