FDA Adverse Event Summary report: N

STEALTHSTATION® I7¿ INTEGRATED NAVIGATION SYSTEM

MDR report key: 3233141 · Received July 18, 2013

Report

Report Number
1723170-2013-00526
Date Received
July 18, 2013
Date of Event
June 21, 2013
Report Date
June 21, 2013
Manufacturer
MEDTRONIC NAVIGATION, INC.
Product Code
HAW
PMA / PMN Number
K050438
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

SOFTWARE INVESTIGATION COMPLETED. THIS ISSUE WILL BE CONTINUALLY MONITORED IN A MEDTRONIC SOFTWARE ANOMALY TRACKING DATABASE.

Additional Manufacturer Narrative · 1

NO PATIENT INFORMATION PROVIDED AS NO PATIENT WAS INVOLVED IN THIS CONCERN. INVESTIGATION HAS NOT BEEN COMPLETED.

Description of Event or Problem · 1

A MEDTRONIC REPRESENTATIVE REPORTED AN UNEXPECTED SOFTWARE EXIT FROM SYNERGY CRANIAL S7. THE NAVIGATION SYSTEM HAD BEEN LEFT ON AT THE NAVIGATE SCREEN OVERNIGHT. THE MEDTRONIC REPRESENTATIVE DID A RE-BOOT AND THE SYSTEM FUNCTIONED NORMALLY. THERE WAS NO PATIENT PRESENT AS THIS OCCURRED OUTSIDE OF A PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
335013 STEALTHSTATION® I7¿ INTEGRATED NAVIGATION SYSTEM NEUROLOGICAL STEREOTAXIC INSTRUMENT HAW MEDTRONIC NAVIGATION, INC. I7

Patients

Seq Age Sex Outcome Treatment
1