FDA Adverse Event Malfunction Summary report: N

AXIUM

MDR report key: 7992251 · Received October 22, 2018

Report

Report Number
2029214-2018-00878
Event Type
Malfunction
Date Received
October 22, 2018
Date of Event
September 24, 2018
Report Date
October 22, 2018
Manufacturer
MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA
Product Code
HCG
PMA / PMN Number
K162704
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VT
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

SEE RELATED REGULATORY REPORTS 2029214-2018-00869, 2029214-2018-00870, 2029214-2018-00872, 2029214-2018-00873, 2029214-2018-00874, 2 029214-2018-00875, 2029214-2018-00877. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
833922 AXIUM DEVICE, NEUROVASCULAR EMBOLIZATION HCG MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA UNK-NV-AXIUM NOT-REP

Patients

Seq Age Sex Outcome Treatment
1