FDA Adverse Event Injury Summary report: N

6000030-2005-00383

MDR report key: 2471498 · Received February 28, 2012

Report

Report Number
6000030-2005-00383
Event Type
Injury
Date Received
February 28, 2012
Date of Event
March 1, 2005
Report Date
August 14, 2025
Manufacturer
MEDTRONIC NEUROMODULATION
PMA / PMN Number
P860004
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Patients

Seq Age Sex Outcome Treatment
1 32 YR Female Hospitalization "SEE H11...."