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

    TOWERLOX PEDICLE SCREW SYSTEM

    K Number: K122332 · Decision Oct 16, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    342
    Registration Numbers
    342
    Same Product Code
    302
    Applicant Total
    7
    Review Days
    75

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    Basic Information

    Device Name
    TOWERLOX PEDICLE SCREW SYSTEM
    K Number
    K122332
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Captiva Spine
    Date Received
    August 2, 2012
    Decision Date
    October 16, 2012
    Product Code
    MNI
    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
    MNI Orthosis, Spinal Pedicle Fixation

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    Other Clearances by Captiva Spine

    K Number Device Name
    K160020 Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System
    K151116 CapLOX II/TowerLOX Pedicle Screw System
    K141332 Captiva Spine SmartLOX Cervical Plate System
    K142586 Captiva Spine FuselOX Cervical IBF System
    K131538 CAPLOX II PEDICLE SCREW SYSTEM/TOWERLOX PEDICLE SCREW SYSTEM
    K122956 FUSELOX LUMBAR INTERBODY FUSION DEVICE