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

    AUTOGENESIS AUTOMATOR, MODEL M1000

    K Number: K013818 · Decision Dec 5, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    66
    Registration Numbers
    66
    Same Product Code
    84
    Applicant Total
    2
    Review Days
    19

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    Basic Information

    Device Name
    AUTOGENESIS AUTOMATOR, MODEL M1000
    K Number
    K013818
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3040
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Autogenesis, Inc.
    Date Received
    November 16, 2001
    Decision Date
    December 5, 2001
    Product Code
    JEC
    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
    JEC Component, Traction, Invasive

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    Other Clearances by Autogenesis, Inc.

    K Number Device Name
    K981423 AUTOGENESIS AUTOMATOR 2000 MODEL NUMBER SC2000