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

    MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM

    K Number: K122571 · Decision Dec 12, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    27
    Review Days
    111

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    Basic Information

    Device Name
    MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM
    K Number
    K122571
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Seaspine, Inc.
    Date Received
    August 23, 2012
    Decision Date
    December 12, 2012
    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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