DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 2182207-2008-00773)
DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 2182207-2008-00773) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEEP BRAIN STIMULATION LEAD; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00773.
| Device | DEEP BRAIN STIMULATION LEAD |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00773 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Study, Literature, Health Professional |
| Narrative | JOURNAL REF: HANDFORTH ET AL. "DEEP BRAIN STIMULATION OF THE SUBTHALAMIC NUCLEUS AS ADJUNCT TREATMENT FOR REFRACTORY EPILEPSY." EPILEPSIA 2006; 47(7): 1239-41. THIS ARTICLE DESCRIBES TWO CASE REPORTS OF BILATERAL SUBTHALAMIC DEEP BRAIN STIMULATION (DBS) FOR REFRACTORY PARTIAL-ONSET EPILEPSY. REPORTABLE EVENT: A FEMALE WITH SEIZURES SINCE AGE 1 YR AFTER HEAD TRAUMA WAS TREATED WITH BILATERAL SUBTHA |
| Source | openFDA MAUDE (device adverse events) |
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