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

    Iliad Pedicle Screw System and Zenius Pedicle Screw System

    K Number: K142835 · Decision Jun 12, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    19
    Review Days
    255

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    Iliad Pedicle Screw System and Zenius Pedicle Screw System
    K Number
    K142835
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medyssey USA, Inc.
    Date Received
    September 30, 2014
    Decision Date
    June 12, 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

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (NKB), ordered by most recent decision date.

    “Socko” Vimax Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ChanPin Pedicle Screw Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Varion Thoracolumbar Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline™ System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AccelFix Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERLA® TL Posterior Thoraco-lumbar Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic
    View all

    Other Clearances by Medyssey USA, Inc.

    K Number Device Name
    K232218 Zenius™ Spinal System
    K230301 Athena III Cervical Plate System
    K223654 Medussa-PL Cage
    K200283 Medussa-PL Cage
    K183407 Triton Cage
    K183409 Athena II Cervical Plate System
    K181978 Zenius™, Iliad™ and Kora™ Spinal Fixation Systems
    K180022 Athena Cervical Plate System
    K170389 TAURUS PEEK Cage System
    K172756 Varian cage
    Search all 19 clearances from Medyssey USA, Inc. →