NEUROPACE RNS SYSTEM DL-330-10 1007605

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 2020-01-21 for NEUROPACE RNS SYSTEM DL-330-10 1007605 manufactured by Neuropace, Inc..

Event Text Entries

[187169924] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[187169925] In (b)(6) 2019, the patient noted a protrusion and some fluid leaking around a portion of the rns system incision site. The patient was scheduled for a revision procedure on (b)(6) 2020. During the procedure, it was determined that one of the unconnected, capped leads was applying outward pressure near the incision line, preventing proper healing. The neurosurgeon re-positioned the lead, securing it away from the incision site. No further information was provided by the treating center.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004426659-2020-00002
MDR Report Key9614122
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-21
Date of Report2020-01-21
Date of Event2019-12-16
Date Mfgr Received2020-01-03
Date Added to Maude2020-01-21
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 94043
Manufacturer CountryUS
Manufacturer Postal94043
Manufacturer Phone6502382788
Manufacturer G1NEUROPACE, INC.
Manufacturer Street455 N. BERNARDO AVE.
Manufacturer CityMOUNTAIN VIEW CA 94043
Manufacturer CountryUS
Manufacturer Postal Code94043
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEUROPACE RNS SYSTEM
Generic NameNEUROPACE RNS SYSTEM
Product CodePFN
Date Received2020-01-21
Model NumberDL-330-10
Catalog Number1007605
Lot Number27875-1-1-1
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNEUROPACE, INC.
Manufacturer Address455 N. BERNARDO AVE. MOUNTAIN VIEW CA 94043 US 94043


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.