BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM

    K Number: K130613 · Decision Jan 22, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    659
    Registration Numbers
    659
    Same Product Code
    1058
    Applicant Total
    2
    Review Days
    321

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    Basic Information

    Device Name
    CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM
    K Number
    K130613
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3040
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Laura Cattabriga
    Date Received
    March 7, 2013
    Decision Date
    January 22, 2014
    Product Code
    HWC
    Advisory Committee
    Orthopedic
    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
    HWC Screw, Fixation, Bone

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    Other Clearances by Laura Cattabriga

    K Number Device Name
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