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

    Curiteva Lumbar Interbody Fusion System

    K Number: K181589 · Decision Dec 20, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    418
    Registration Numbers
    418
    Same Product Code
    890
    Applicant Total
    4
    Review Days
    185

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    Basic Information

    Device Name
    Curiteva Lumbar Interbody Fusion System
    K Number
    K181589
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3080
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Curiteva, LLC
    Date Received
    June 18, 2018
    Decision Date
    December 20, 2018
    Product Code
    MAX
    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
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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    Other Clearances by Curiteva, LLC

    K Number Device Name
    K181549 Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System)
    K181562 Curiteva Anterior Cervical Plate System
    K181261 Curiteva Cervical Interbody Fusion System