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...."