NEUROPACE RNS SYSTEM RNS-320-K 1007694

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 2020-03-24 for NEUROPACE RNS SYSTEM RNS-320-K 1007694 manufactured by Neuropace, Inc..

MAUDE Entry Details

Report Number3004426659-2020-00012
MDR Report Key9875782
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-24
Date of Report2020-03-24
Date of Event2020-02-27
Date Mfgr Received2020-02-27
Date Added to Maude2020-03-24
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 ContactMRS. RAMONA GONIS
Manufacturer Street455 N. BERNARDO AVE.
Manufacturer CityMOUNTAIN VIEW, CA
Manufacturer CountryUS
Manufacturer Phone2382788
Manufacturer G1NEUROPACE, INC.
Manufacturer Street455 N. BERNARDO AVE.
Manufacturer CityMOUNTAIN VIEW, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEUROPACE RNS SYSTEM
Generic NameNEUROPACE RNS SYSTEM
Product CodePFN
Date Received2020-03-24
Model NumberRNS-320-K
Catalog Number1007694
Lot Number26328-1-1-1
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNEUROPACE, INC.
Manufacturer Address455 N. BERNARDO AVE. MOUNTAIN VIEW, CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-03-24

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