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

    Redi-Spine

    K Number: K181584 · Decision Aug 10, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    407
    Registration Numbers
    407
    Same Product Code
    900
    Applicant Total
    7
    Review Days
    56

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    Basic Information

    Device Name
    Redi-Spine
    K Number
    K181584
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Innovative Surgical Designs, Inc.
    Date Received
    June 15, 2018
    Decision Date
    August 10, 2018
    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 Innovative Surgical Designs, Inc.

    K Number Device Name
    K220297 True Tulip, True M.I.S.
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    K201780 True Tulip System, True M.I.S. System
    K171559 True Spinal Fixation System
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