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

    KMC KYPHOPLASTY SYSTEM

    K Number: K113742 · Decision Sep 17, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    114
    Registration Numbers
    114
    Same Product Code
    107
    Applicant Total
    1
    Review Days
    272

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    Basic Information

    Device Name
    KMC KYPHOPLASTY SYSTEM
    K Number
    K113742
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3027
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Shanghai Kinetic Medical Co., Ltd.
    Date Received
    December 20, 2011
    Decision Date
    September 17, 2012
    Product Code
    NDN
    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
    NDN Cement, Bone, Vertebroplasty

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