FDA Adverse Event Injury Summary report: N

TIBIAL INSERT

MDR report key: 232684 · Received July 7, 1999

Report

Report Number
1043534-1999-00057
Event Type
Injury
Date Received
July 7, 1999
Date of Event
May 25, 1999
Manufacturer
WRIGHT MED TECHNOLOGY, INC
Product Code
HSH
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TIBIAL INSERT Implant KNEE COMPONENT HSH WRIGHT MED TECHNOLOGY, INC NA NA

Patients

Seq Age Sex Outcome Treatment
1