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

    HYDRALOK SYSTEM

    K Number: K051216 · Decision Jul 19, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    338
    Registration Numbers
    338
    Same Product Code
    308
    Applicant Total
    5
    Review Days
    68

    Basic Information

    Device Name
    HYDRALOK SYSTEM
    K Number
    K051216
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    ALTIVA CORP.
    Date Received
    May 12, 2005
    Decision Date
    July 19, 2005
    Product Code
    MNH
    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
    MNH Orthosis, Spondylolisthesis Spinal Fixation

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