FDA Adverse Event Injury Summary report: N

2020394-1997-00005

MDR report key: 108641 · Received July 25, 1997

Report

Report Number
2020394-1997-00005
Event Type
Injury
Date Received
July 25, 1997
Date of Event
June 18, 1997
Product Code
DSY
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 Implant DSY

Patients

Seq Age Sex Outcome Treatment
1