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    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    WASTON General Spinal System

    K Number: K150684 · Decision Nov 18, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    342
    Registration Numbers
    342
    Same Product Code
    302
    Applicant Total
    5
    Review Days
    246

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    Basic Information

    Device Name
    WASTON General Spinal System
    K Number
    K150684
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Changzhou Waston Medical Appliance Co., Ltd.
    Date Received
    March 17, 2015
    Decision Date
    November 18, 2015
    Product Code
    MNI
    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
    MNI Orthosis, Spinal Pedicle Fixation

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