OVATION IX TV-IL1412120-J

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-30 for OVATION IX TV-IL1412120-J manufactured by Endologix Santa Rosa.

MAUDE Entry Details

Report Number3008011247-2020-00048
MDR Report Key9901836
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-30
Date of Report2020-03-02
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Date Added to Maude2020-03-30
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 FDA3
Event Location3
Manufacturer ContactMR. EMILE PINSONNEAULT
Manufacturer Street2 MUSICK ,
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone8009832284
Manufacturer G1ENDOLOGIX
Manufacturer Street2 MUSICK ,
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal Code92618
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOVATION IX
Generic NameILIAC LIMB
Product CodeMIH
Date Received2020-03-30
Model NumberTV-IL1412120-J
Lot NumberFS040119-12
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerENDOLOGIX SANTA ROSA
Manufacturer Address3910 BRICKWAY BLVD , SANTA ROSA CA 95403 US 95403


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-30

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