DEEP BRAIN STIMULATOR LEAD Adverse Event — Death (MDR 2182207-2008-00731)
DEEP BRAIN STIMULATOR LEAD Adverse Event — Death (MDR 2182207-2008-00731) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEEP BRAIN STIMULATOR LEAD; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00731.
| Device | DEEP BRAIN STIMULATOR LEAD |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00731 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Study, Literature, Health Professional |
| Narrative | JOURNAL REFERENCE: MCCLELLAND ET AL. "RELATIONSHIP OF CLINICAL EFFICACY TO POSTMORTEM-DETERMINED ANATOMIC SUBTHALAMIC STIMULATION IN PARKINSON SYNDROME." CLIN NEUROPATHOL 2007; 26(6); 267-275. THIS ARTICLE DESCRIBES A MALE WITH PARKINSON'S DISEASE WHO WAS PROSPECTIVELY FOLLOWED IN A LONG-TERM CLINICAL PROTOCOL UNTIL HIS DEATH, 40 MOS AFTER ELECTRODE PLACEMENT. AFTER NON-DEVICE RELATED DEATH, THE A |
| Source | openFDA MAUDE (device adverse events) |
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