FDA Adverse Event Injury Summary report: N

DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD

MDR report key: 285085 · Received June 20, 2000

Report

Report Number
1043534-1999-00089
Event Type
Injury
Date Received
June 20, 2000
Date of Event
August 30, 1999
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
KRP
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT/EXTD KNEE COMPONENT KRP WRIGHT MEDICAL TECHNOLOGY, INC. NA 048A079500

Patients

Seq Age Sex Outcome Treatment
1