FDA Adverse Event Malfunction Summary report: N

1043534-2012-01059

MDR report key: 2853400 · Received November 30, 2012

Report

Report Number
1043534-2012-01059
Event Type
Malfunction
Date Received
November 30, 2012
Report Date
August 17, 2012
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
PMA / PMN Number
P030027
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER
Health Professional
*

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown