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

    APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE

    K Number: K141041 · Decision May 16, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    6
    Applicant Total
    1
    Review Days
    23

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    Basic Information

    Device Name
    APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE
    K Number
    K141041
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.3460
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Aptus Endosystems
    Date Received
    April 23, 2014
    Decision Date
    May 16, 2014
    Product Code
    OTD
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OTD Endovascular Suturing System

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