ELEOS DISTAL FEMUR AXIAL PIN 25002111E

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 2020-03-23 for ELEOS DISTAL FEMUR AXIAL PIN 25002111E manufactured by Onkos Surgical.

Event Text Entries

[186189285] This report is for one of three devices involved in this event, please refer to report 3013450937-2020-00037 and 3013450937-2020-00038. The device history record and sterilization batch release record were reviewed and indicated that the component involved met specification. The component was unable to be obtained for further analysis. Should additional information be obtained the report will be supplemented.
Patient Sequence No: 1, Text Type: N, H10


[186189286] The patient underwent a revision surgery due to an alleged infection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3013450937-2020-00036
MDR Report Key9865213
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-23
Date of Report2020-03-23
Date of Event2018-02-26
Date Mfgr Received2020-02-24
Device Manufacturer Date2017-03-14
Date Added to Maude2020-03-23
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 ContactCRISTINA BUTRICO
Manufacturer Street77 EAST HALSEY ROAD
Manufacturer CityPARSIPPANY, NJ
Manufacturer CountryUS
Manufacturer Phone2645433
Manufacturer G1MICROPORT ORTHOPEDIC
Manufacturer Street5677 AIRLINE ROAD
Manufacturer CityARLINGTON, TN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELEOS DISTAL FEMUR AXIAL PIN
Generic NamePROSTHESIS, KNEE
Product CodeKRO
Date Received2020-03-23
Model Number25002111E
Catalog Number25002111E
Lot Number1701668
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerONKOS SURGICAL
Manufacturer Address77 EAST HALSEY ROAD PARSIPPANY, NJ US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-23

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