BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

    Mega Plus Spine System

    K Number: K173180 · Decision Mar 15, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    11
    Review Days
    167

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    Basic Information

    Device Name
    Mega Plus Spine System
    K Number
    K173180
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bk Meditech, Co., Ltd.
    Date Received
    September 29, 2017
    Decision Date
    March 15, 2018
    Product Code
    NKB
    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
    NKB Thoracolumbosacral Pedicle Screw System

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    Other Clearances by Bk Meditech, Co., Ltd.

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    K110426 DYNA-EXTOR II
    K090424 DVX SPINE SYSTEM
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