BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    7D Surgical System - Percutaneous Application (7D Flash Frame)

    K Number: K220522 · Decision May 20, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    370
    Registration Numbers
    370
    Same Product Code
    404
    Applicant Total
    1
    Review Days
    86

    Basic Information

    Device Name
    7D Surgical System - Percutaneous Application (7D Flash Frame)
    K Number
    K220522
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    882.4560
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    7D Surgical
    Date Received
    February 23, 2022
    Decision Date
    May 20, 2022
    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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