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

    NuVasive Reline System

    K Number: K143684 · Decision Apr 23, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    413
    Registration Numbers
    413
    Same Product Code
    873
    Applicant Total
    7
    Review Days
    120

    Basic Information

    Device Name
    NuVasive Reline System
    K Number
    K143684
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    NUVASIVE INCORPORATED
    Date Received
    December 24, 2014
    Decision Date
    April 23, 2015
    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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