VERTE-STACK SPINAL SYSTEM Adverse Event — Malfunction (MDR 1030489-2008-00081)
VERTE-STACK SPINAL SYSTEM Adverse Event — Malfunction (MDR 1030489-2008-00081) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VERTE-STACK SPINAL SYSTEM; Generic name: VB REPLACEMENT; Manufacturer: SOFAMOR DANEK DEGGENDORF GMBH.
| Device | VERTE-STACK SPINAL SYSTEM |
|---|---|
| Generic name | VB REPLACEMENT |
| Manufacturer | SOFAMOR DANEK DEGGENDORF GMBH |
| Report number | 1030489-2008-00081 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT A VERTEBRAL SPACER CRACKED DURING INSERTION. TWO THIRDS OF THE BROKEN DEVICE WAS IMPLANTED. NO PT COMPLICATIONS WERE REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →