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EBI ANTERIOR CERVICAL PLATE SYSTEM Adverse Event — Malfunction (MDR 2242816-2008-00004)

EBI ANTERIOR CERVICAL PLATE SYSTEM Adverse Event — Malfunction (MDR 2242816-2008-00004) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EBI ANTERIOR CERVICAL PLATE SYSTEM; Manufacturer: EBI; Report number: 2242816-2008-00004.

DeviceEBI ANTERIOR CERVICAL PLATE SYSTEM
ManufacturerEBI
Report number2242816-2008-00004
Event typeMalfunction
Product problemY
Date received2008-02-14
Report sourceHealth Professional
NarrativeA BROKEN SCREW AT C4 WAS REPORTED. THE SCREW REMAINS IMPLANTED, PATIENT STATUS IS GOOD.
SourceopenFDA MAUDE (device adverse events)

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