FDA Adverse Event Malfunction Summary report: N

STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

MDR report key: 2081247 · Received April 21, 2011

Report

Report Number
1723170-2011-00825
Event Type
Malfunction
Date Received
April 21, 2011
Date of Event
May 10, 2010
Report Date
June 8, 2010
Manufacturer
MEDTRONIC NAVIGATION, INC.
Product Code
HAW
PMA / PMN Number
K050438
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

SOFTWARE INVESTIGATION SHOWS POOR TRACING TECHNIQUE FROM SURGEON. SOFTWARE BEHAVING AS DESIGNED.

Description of Event or Problem · 1

SITE ALLEGED AN INACCURACY DURING PT REGISTRATION. THEY WERE ABLE TO SWITCH FROM TRACER TO A POINT MERGE FOR A SUCCESSFUL REGISTRATION. NO IMPACT ON PT OUTCOME REPORTED.

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