POST CRANIOTOMY SUBDURAL Adverse Event — Malfunction (MDR 2023988-2008-00006)
POST CRANIOTOMY SUBDURAL Adverse Event — Malfunction (MDR 2023988-2008-00006) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: POST CRANIOTOMY SUBDURAL; Generic name: NONE; Manufacturer: INTEGRA NEURO SCIENCES.
| Device | POST CRANIOTOMY SUBDURAL |
|---|---|
| Generic name | NONE |
| Manufacturer | INTEGRA NEURO SCIENCES |
| Report number | 2023988-2008-00006 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Foreign, Distributor |
| Narrative | TO DATE, THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS NOT BEEN RECEIVED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFO. |
| Source | openFDA MAUDE (device adverse events) |
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