DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 2182207-2008-00769)
DEEP BRAIN STIMULATION LEAD Adverse Event — Injury (MDR 2182207-2008-00769) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEEP BRAIN STIMULATION LEAD; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00769.
| Device | DEEP BRAIN STIMULATION LEAD |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00769 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Foreign, Study, Literature, Health Professional |
| Narrative | JOURNAL REF: PATRICK ET AL. "DEEP BRAIN STIMULATION OF THE INTERNAL PALLIDUM IN MULTIPLE SYS ATROPHY - CASE REPORT" PARKINSONISM & RELATED DISORDERS/2006/12/181-183. THE ARTICLE IS A CASE STUDY OF ONE MALE PT WITH MULTIPLE SYS ATROPHY WHO WAS TREATED WITH BILATERAL DBS OF THE INTERNAL PALLIDUM. AT 4 MONTHS HIS AXIAL DYSTONIA CHANGED TO AN EXTENSION DYSTONIC POSTURE WITH A TENDENCY TOWARD RETROCOLL |
| Source | openFDA MAUDE (device adverse events) |
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