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

    Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection

    K Number: K181529 · Decision Dec 6, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    402
    Applicant Total
    2
    Review Days
    178

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    Basic Information

    Device Name
    Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection
    K Number
    K181529
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Contego Medical, LLC
    Date Received
    June 11, 2018
    Decision Date
    December 6, 2018
    Product Code
    LIT
    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
    LIT Catheter, Angioplasty, Peripheral, Transluminal

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    Other Clearances by Contego Medical, LLC

    K Number Device Name
    K181128 Paladin Carotid Post-dilation Balloon System with Integrated Embolic Protection (Paladin System)