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

    LAGUNA POLYAXIAL PEDICLE SCREW SYSTEM

    K Number: K083826 · Decision Jan 22, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    326
    Registration Numbers
    326
    Same Product Code
    308
    Applicant Total
    7
    Review Days
    30

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    Basic Information

    Device Name
    LAGUNA POLYAXIAL PEDICLE SCREW SYSTEM
    K Number
    K083826
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Allez Spine, LLC
    Date Received
    December 23, 2008
    Decision Date
    January 22, 2009
    Product Code
    MNH
    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
    MNH Orthosis, Spondylolisthesis Spinal Fixation

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    K070460 ALLEZ SPINE CROSS CONNECTORS
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