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

    FLEXCEL CAROTID SHUNT (INLYING), MODEL 2020-05

    K Number: K071367 · Decision Aug 29, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    89
    Applicant Total
    32
    Review Days
    105

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    Basic Information

    Device Name
    FLEXCEL CAROTID SHUNT (INLYING), MODEL 2020-05
    K Number
    K071367
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.4450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    LeMaitre Vascular, Inc.
    Date Received
    May 16, 2007
    Decision Date
    August 29, 2007
    Product Code
    MJN
    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
    MJN Catheter, Intravascular Occluding, Temporary

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