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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MONTERIS MEDICAL NEUROBLATE® SYSTEM
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MONTERIS MEDICAL NEUROBLATE® SYSTEM Back to Search Results
Model Number 20360
Medical Device Problem Code Computer Software Problem (1112)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Date of Event 10/17/2018
Type of Reportable Event Malfunction
Event or Problem Description
It was reported that during an ablation procedure, cold pixels were witnessed approximately 15mm from the probe.It was noted that the user let off the foot pedal once the pixels were witnessed.The physician performed a biopsy prior to the ablation procedure but did not flush with a solution.There were no patient complications reported in relation to this event.
 
Additional Manufacturer Narrative
The blue pixels in this case were accompanied by a reduction in the magnitude signal in the area.This is not an instance of "cold pixels" event but rather a drop in magnitude causing issues with the phase data which were interpreted as temperature.
 
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Brand Name
NEUROBLATE® SYSTEM
Common Device Name
NEUROBLATE® SYSTEM
Manufacturer (Section D)
MONTERIS MEDICAL
14755 27th ave n
suite c
plymouth MN 55447
MDR Report Key8005235
Report Number3009970070-2018-00085
Device Sequence Number202985
Product Code GEX
UDI-Device Identifier00816589020656
UDI-Public00816589020656
Combination Product (Y/N)N
Initial Reporter StateMN
Initial Reporter CountryUS
PMA/510(K) Number
K173305
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial,Followup
Report Date (Section B) 10/25/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model Number20360
Device Catalogue NumberNB102
Was Device Available for Evaluation? Yes
Initial Date Received by Manufacturer 10/17/2018
Supplement Date Received by Manufacturer10/29/2018
Initial Report FDA Received Date10/25/2018
Supplement Report FDA Received Date10/30/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
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