EBI SPINELINK SPINAL FIXATION SYSTEM Adverse Event — Malfunction (MDR 2242816-2008-00021)
EBI SPINELINK SPINAL FIXATION SYSTEM Adverse Event — Malfunction (MDR 2242816-2008-00021) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EBI SPINELINK SPINAL FIXATION SYSTEM; Generic name: NKB; Manufacturer: EBI.
| Device | EBI SPINELINK SPINAL FIXATION SYSTEM |
|---|---|
| Generic name | NKB |
| Manufacturer | EBI |
| Report number | 2242816-2008-00021 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT A SCREW IN S1 HAS FRACTURED. PT IS ASYMPTOMATIC. |
| Source | openFDA MAUDE (device adverse events) |
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