BAXANO NEUROLOCALIZATION RIBBON FG0866-02

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2009-06-16 for BAXANO NEUROLOCALIZATION RIBBON FG0866-02 manufactured by Baxano, Inc..

Event Text Entries

[16486196] (b) (4). ( device short). The device was returned for inspection. Electrical short was noticed in the area of the printed circuit board. The manufacturing procedure was revised to include adding a uv adhesive to insulate the printed circuit board face.
Patient Sequence No: 1, Text Type: N, H10


[16703716] Following a standard decompression at the l4-5 disc level, the physician pulled the neurolocalization ribbon through the left-sided l4 foramen, applied current to localize the nerve root, and achieved desired responses. The physician then attempted to stimulate the nerve out the right-side of the l4 foramen, but no response was achieved when current applied. The device was returned for evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006324586-2009-00008
MDR Report Key1471588
Report Source05
Date Received2009-06-16
Date of Report2009-06-16
Date of Event2009-05-27
Date Mfgr Received2009-05-27
Device Manufacturer Date2009-05-01
Date Added to Maude2010-03-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactPATTY HEVEY
Manufacturer Street2660 MARINE WAY, SUITE B
Manufacturer CityMOUNTAIN VIEW CA 94043
Manufacturer CountryUS
Manufacturer Postal94043
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBAXANO NEUROLOCALIZATION RIBBON
Generic NameNONE
Product CodeGZI
Date Received2009-06-16
Returned To Mfg2009-05-29
Catalog NumberFG0866-02
Lot Number09050801
Device Expiration Date2009-11-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBAXANO, INC.
Manufacturer Address2660 MARINE WAY, SUITE B MOUNTAIN VIEW CA 94043 US 94043


Patients

Patient NumberTreatmentOutcomeDate
10 2009-06-16

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