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

    SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES

    K Number: K072672 · Decision Nov 28, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    13
    Review Days
    68

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    Basic Information

    Device Name
    SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
    K Number
    K072672
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Abbott Spine, Inc.
    Date Received
    September 21, 2007
    Decision Date
    November 28, 2007
    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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