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    FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

    360CAS Knee

    K Number: K242009 · Decision Aug 8, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    381
    Registration Numbers
    381
    Same Product Code
    430
    Applicant Total
    2
    Review Days
    29

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    Basic Information

    Device Name
    360CAS Knee
    K Number
    K242009
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    882.4560
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kico Knee Innovation Company Pty, Ltd.
    Date Received
    July 10, 2024
    Decision Date
    August 8, 2024
    Product Code
    OLO
    Advisory Committee
    Neurology
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OLO Orthopedic Stereotaxic Instrument

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    Other Clearances by Kico Knee Innovation Company Pty, Ltd.

    K Number Device Name
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