FDA Adverse Event Injury Summary report: N

1627487-2010-01532

MDR report key: 1790629 · Received August 6, 2010

Report

Report Number
1627487-2010-01532
Event Type
Injury
Date Received
August 6, 2010
Date of Event
December 8, 2009
Report Date
July 30, 2013
Manufacturer
ADVANCED NEUROMODULATION SYSTEMS
PMA / PMN Number
P010032
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
NOT APPLICABLE
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 NA Female Required Intervention