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

    MODIFICATION TO SPIRAL RADIUS 90-D SST SYSTEM

    K Number: K021825 · Decision Jul 1, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    321
    Same Product Code
    429
    Applicant Total
    2
    Review Days
    27

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    Basic Information

    Device Name
    MODIFICATION TO SPIRAL RADIUS 90-D SST SYSTEM
    K Number
    K021825
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3050
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Unitedstates Surgical
    Date Received
    June 4, 2002
    Decision Date
    July 1, 2002
    Product Code
    KWP
    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
    KWP Appliance, Fixation, Spinal Interlaminal

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