NEUROFORM ATLAS STENT SYSTEM 3.0 X 15MM WITHOUT TIP M003EZAS30150

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a study report with the FDA on 2020-01-22 for NEUROFORM ATLAS STENT SYSTEM 3.0 X 15MM WITHOUT TIP M003EZAS30150 manufactured by Stryker Neurovascular Cork.

Event Text Entries

[176100438] This is the first of 2 reports. Subject device remains implanted.
Patient Sequence No: 1, Text Type: N, H10


[176100439] It was reported that during stent-assisted coiling of an aneurysm located at the left posterior cerebral at basilar, the subject stent was properly implanted at desired place. When packing the aneurysm sac with coils through a microcatheter, the microcatheter expelled, generating loops of coils between the meshes of the stent. It was confirmed that recanalization was a consequence of the extrusion. There were no clinical consequences to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008881809-2020-00014
MDR Report Key9618122
Report SourceSTUDY
Date Received2020-01-22
Date of Report2020-02-21
Date of Event2017-03-06
Date Mfgr Received2020-01-29
Device Manufacturer Date2016-08-17
Date Added to Maude2020-01-22
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. TARA LOPEZ
Manufacturer Street47900 BAYSIDE PARKWAY
Manufacturer CityFREMONT CA 94538
Manufacturer CountryUS
Manufacturer Postal94538
Manufacturer Phone5104132500
Manufacturer G1STRYKER NEUROVASCULAR CORK
Manufacturer StreetIDA INDUSTRIAL ESTATE MODEL FARM ROAD
Manufacturer CityCORK NA
Manufacturer CountryIE
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEUROFORM ATLAS STENT SYSTEM 3.0 X 15MM WITHOUT TIP
Generic NameSTENT, INTRACRANIAL NEUROVASCULAR
Product CodeNJE
Date Received2020-01-22
Catalog NumberM003EZAS30150
Lot Number19248216
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER NEUROVASCULAR CORK
Manufacturer AddressIDA INDUSTRIAL ESTATE MODEL FARM ROAD CORK NA IE NA


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-22

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