FDA Adverse Event Malfunction Summary report: N

STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

MDR report key: 2093630 · Received April 6, 2011

Report

Report Number
1723170-2011-00753
Event Type
Malfunction
Date Received
April 6, 2011
Date of Event
March 8, 2011
Report Date
March 8, 2011
Manufacturer
MEDTRONIC NAVIGATION, INC.
Product Code
HAW
PMA / PMN Number
K050438
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

NO PATIENT WAS PRESENT. INVESTIGATION IS CURRENTLY IN PROGRESS.

Description of Event or Problem · 1

A SITE REPRESENTATIVE REPORTED AN ISSUE WITH INTERMITTENT TRACKING WITH A CAMERA ON A STEALTHSTATION. THERE WAS NO PATIENT PRESENT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1