FDA Adverse Event Malfunction Summary report: N

1043534-2012-01184

MDR report key: 2850775 · Received November 29, 2012

Report

Report Number
1043534-2012-01184
Event Type
Malfunction
Date Received
November 29, 2012
Report Date
September 19, 2012
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
PMA / PMN Number
P030027
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
PATIENT
Health Professional
*

Patients

Seq Age Sex Outcome Treatment
1 79 YR Female