BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ELEOS LIMB SALVAGE SYSTEM

    MDR report key: 19577038 · Received June 20, 2024

    Report

    Report Number
    3013450937-2024-00193
    Event Type
    Injury
    Date Received
    June 20, 2024
    Date of Event
    May 20, 2024
    Report Date
    June 20, 2024
    Manufacturer
    ONKOS SURGICAL
    Product Code
    KRO
    UDI-DI
    B27825002112E0
    PMA / PMN Number
    K161520
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE ROOT CAUSE OF THIS COMPLAINT WAS NOT DETERMINED. BASED ON THE REVIEW OF DEVICE HISTORY RECORDS, THE INVESTIGATION CONCLUDED THAT THE ROOT CAUSE OF THE ALLEGED INFECTION WAS NOT RELATED TO THE DESIGN, MANUFACTURE, AND/OR STERILIZATION OF THE EXPLANTED ELEOS DEVICES.

    Description of Event or Problem · 0

    IT WAS REPORTED BY S. STEINERT, AN ONKOS SALES REPRESENTATIVE, THAT A 74-YEAR-OLD FEMALE PATIENT WITH AN ELEOS HINGE KNEE REPLACEMENT UNDERWENT A REVISION SURGERY ON (B)(6) 2024 DUE TO AN ALLEGED INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1512238 ELEOS LIMB SALVAGE SYSTEM RESURFACING FEMUR AXIAL PIN KRO ONKOS SURGICAL 1700370 B27825002112E0

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Female Required Intervention RESURFACING FEMUR AXIAL PIN| TIBIAL POLY SPACER| TIBIAL ROTATIONAL HINGE