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

    DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage

    K Number: K162220 · Decision Nov 21, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    339
    Registration Numbers
    339
    Same Product Code
    348
    Applicant Total
    7
    Review Days
    105

    Basic Information

    Device Name
    DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage
    K Number
    K162220
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3080
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Dio Medical Co., Ltd.
    Date Received
    August 8, 2016
    Decision Date
    November 21, 2016
    Product Code
    ODP
    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
    ODP Intervertebral Fusion Device With Bone Graft, Cervical

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