FDA Adverse Event
Injury
Summary report: N
6000030-2007-00156
MDR report key: 2843015
·
Received November 21, 2012
Report
- Report Number
- 6000030-2007-00156
- Event Type
- Injury
- Date Received
- November 21, 2012
- Date of Event
- October 11, 2005
- Report Date
- August 15, 2025
- Manufacturer
- MEDTRONIC NEUROMODULATION
- PMA / PMN Number
- P860004
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- 003
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 63 YR | Male | Required Intervention| S | "SEE H11...." |