FDA Adverse Event Malfunction Summary report: N

GREENLIGHT ADDSTAT

MDR report key: 1880143 · Received October 13, 2010

Report

Report Number
2937094-2010-00724
Event Type
Malfunction
Date Received
October 13, 2010
Date of Event
September 14, 2010
Report Date
September 14, 2010
Manufacturer
AMS, INNOVATION CENTER - SILICON VALLEY
Product Code
GEX
PMA / PMN Number
K062719
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY THE CUSTOMER THAT ON (B)(6) 2010, AN AIMING BEAM FIRED STRAIGHT OUT OF THE FIBER AT 6,586 JOULES. A DEVICE EVALUATION IS PENDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMS, INNOVATION CENTER - SILICON VALLEY NA 023H

Patients

Seq Age Sex Outcome Treatment
1 Other