FDA Adverse Event Malfunction Summary report: N

STEALTHSTATION TRIA NAVIGATION SYSTEM

MDR report key: 2050098 · Received April 1, 2011

Report

Report Number
1723170-2011-00558
Event Type
Malfunction
Date Received
April 1, 2011
Date of Event
February 25, 2010
Report Date
February 25, 2010
Manufacturer
MEDTRONIC NAVIGATION, INC.
Product Code
HAW
PMA / PMN Number
K001153
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

NO PT WAS PRESENT AT THE TIME THIS MALFUNCTION OCCURRED. THE COMPUTER WAS REPLACED AND THIS RESOLVED THE ISSUE. THE HARD DRIVE MALFUNCTION DIRECTLY CAUSED THE EVENT.

Description of Event or Problem · 1

MEDTRONIC REP REPORTED THAT AFTER SELECTING A PROCEDURE (FLURO IMAGING WITH OPTICAL TRACKING), THE SOFTWARE FREEZES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 STEALTHSTATION TRIA NAVIGATION SYSTEM STEREOTAXIC INSTRUMENT (HAW) HAW MEDTRONIC NAVIGATION, INC. TRIA NA

Patients

Seq Age Sex Outcome Treatment
1