FDA Adverse Event Injury Summary report: N

FOUNDATION KNEE TIBIA INSERT

MDR report key: 183269 · Received August 20, 1998

Report

Report Number
1644408-1998-00004
Event Type
Injury
Date Received
August 20, 1998
Date of Event
June 1, 1998
Report Date
August 18, 1998
Manufacturer
ENCORE ORTHOPAEDICS, INC.
Product Code
HRY
Adverse Event
Yes
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FOUNDATION KNEE TIBIA INSERT Implant TIBIA INSERT HRY ENCORE ORTHOPAEDICS, INC. 62431

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization