FLANGE FIXTURE 4MM SEC 002-0 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-05-13 for FLANGE FIXTURE 4MM SEC 002-0 N/A manufactured by Cochlear Bone Anchored Solutions Ab.

Event Text Entries

[144921562] This report is submitted on may 14, 2019. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[144921563] It was reported that the patient's device was electively explanted (date not reported) due to a traumatic injury. The patient will not be re-implanted with a new device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000034-2019-00724
MDR Report Key8606310
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-05-13
Date of Report2019-04-19
Date Mfgr Received2019-04-19
Date Added to Maude2019-05-13
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. KRISTEL KOHNE
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 NameFLANGE FIXTURE 4MM
Generic NameNOBEL BIOCARE AB - PROSTHESIS
Product CodeFZE
Date Received2019-05-13
Model NumberSEC 002-0
Catalog NumberN/A
Lot NumberN/A
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 2019-05-13

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