FDA Adverse Event Injury Summary report: N

1043534-2012-01242

MDR report key: 2885797 · Received December 26, 2012

Report

Report Number
1043534-2012-01242
Event Type
Injury
Date Received
December 26, 2012
Date of Event
June 15, 2009
Report Date
September 21, 2012
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC
PMA / PMN Number
K021489
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Patients

Seq Age Sex Outcome Treatment
1 NA Male Required Intervention