FDA Adverse Event Malfunction Summary report: N

VERTEBRON PSS TORQUE INDICATING SCREW DRIVER

MDR report key: 939179 · Received September 2, 2004

Report

Report Number
3004435519-2004-00002
Event Type
Malfunction
Date Received
September 2, 2004
Manufacturer
VERTEBRON, INC.
Product Code
HXX
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERTEBRON PSS TORQUE INDICATING SCREW DRIVER SCREW DRIVER HXX VERTEBRON, INC. 900-1018 T0070804

Patients

Seq Age Sex Outcome Treatment
1 YR