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

    MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM

    K Number: K012305 · Decision Aug 22, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    356
    Registration Numbers
    356
    Same Product Code
    665
    Applicant Total
    7
    Review Days
    30

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    Basic Information

    Device Name
    MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
    K Number
    K012305
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3060
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sulzer Spine-Tech
    Date Received
    July 23, 2001
    Decision Date
    August 22, 2001
    Product Code
    KWQ
    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
    KWQ Appliance, Fixation, Spinal Intervertebral Body

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