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

    VertiForm Posterior Fixation System

    K Number: K161499 · Decision Jul 29, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    6
    Review Days
    58

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    Basic Information

    Device Name
    VertiForm Posterior Fixation System
    K Number
    K161499
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Next Orthosurgical
    Date Received
    June 1, 2016
    Decision Date
    July 29, 2016
    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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    Other Clearances by Next Orthosurgical

    K Number Device Name
    K242509 HAnano InterFuse(R) Modular Interbody
    K190981 NEX-D2 Posterior Fixation System
    K161608 InterForm Cervical Interbody Cage System
    K141291 VERTIFORM POSTERIOR FIXATION SYSTEM
    K131082 INTERFORM INTERBODY CAGE SYSTEM