VERTEX RECONSTRUCTION SYSTEM Adverse Event — Malfunction (MDR 1030489-2008-00073)
VERTEX RECONSTRUCTION SYSTEM Adverse Event — Malfunction (MDR 1030489-2008-00073) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VERTEX RECONSTRUCTION SYSTEM; Generic name: CROSSLINK; Manufacturer: WARSAW ORTHOPEDIC INC..
| Device | VERTEX RECONSTRUCTION SYSTEM |
|---|---|
| Generic name | CROSSLINK |
| Manufacturer | WARSAW ORTHOPEDIC INC. |
| Report number | 1030489-2008-00073 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Company representation, COMPANY REPRESENTATIVE |
| Source | openFDA MAUDE (device adverse events) |
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