BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    GALILEOS IMPLANT, V 1.0

    K Number: K061472 · Decision Jun 9, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    7
    Review Days
    10

    Basic Information

    Device Name
    GALILEOS IMPLANT, V 1.0
    K Number
    K061472
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    SICAT GMBH & CO. KG
    Date Received
    May 30, 2006
    Decision Date
    June 9, 2006
    Product Code
    LLZ
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    LLZ System, Image Processing, Radiological

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    Other Clearances by SICAT GMBH & CO. KG

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