FDA Adverse Event Injury Summary report: N

1043534-2012-01176

MDR report key: 2851098 · Received November 29, 2012

Report

Report Number
1043534-2012-01176
Event Type
Injury
Date Received
November 29, 2012
Date of Event
December 14, 2010
Report Date
September 19, 2012
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
PMA / PMN Number
K931333
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER
Health Professional
*

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention