COCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM 93101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-01-24 for COCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM 93101 manufactured by Cochlear Bone Anchored Solutions Ab.

Event Text Entries

[98044142] This report is submitted on (b)(6) 2018, by (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[98044143] Per the clinic, the patient experienced a loss of osseointegration resulting in fixture loss, subsequent to sustaining a trauma to the implant site. It is unknown if there are plans to reimplant the patient as of the date of this report (b)(6) 2018.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000034-2018-00220
MDR Report Key7214566
Report SourceHEALTH PROFESSIONAL
Date Received2018-01-24
Date of Report2018-01-14
Date Mfgr Received2018-01-14
Date Added to Maude2018-01-24
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 ContactMS. SUJEEWA WIJESINGHE
Manufacturer Street1 UNIVERSITY AVENUE
Manufacturer CityMACQUARIE UNIVERSITY, NSW 2109
Manufacturer CountryAS
Manufacturer Postal2109
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM
Generic NameCOCHLEAR BAHA CONNECT SYSTEM
Product CodeFZE
Date Received2018-01-24
Model Number93101
Catalog Number93101
Lot NumberASKU
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOCHLEAR BONE ANCHORED SOLUTIONS AB
Manufacturer AddressKONSTRUKTIONSV?GEN 14 PO BOX 82 M?LNLYCKE, 435 22 SW 435 22


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-01-24

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