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

    ALEXIS WOUND RETRACTOR, MODELS C8312, C8301, C8302, C8303, C8304

    K Number: K041711 · Decision Aug 26, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    8
    Applicant Total
    45
    Review Days
    64

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    Basic Information

    Device Name
    ALEXIS WOUND RETRACTOR, MODELS C8312, C8301, C8302, C8303, C8304
    K Number
    K041711
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4370
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Applied Medical Resources Corp.
    Date Received
    June 23, 2004
    Decision Date
    August 26, 2004
    Product Code
    KGW
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KGW Ring (Wound Protector), Drape Retention, Internal

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (KGW), ordered by most recent decision date.

    Alexis lighted wound protector-retractor, flexible, extra small (cl312);Alexis lighted wound protector-retractor, flexible, small (cl301);Alexis lighted wound protector-retractor, flexible, medium (cl302);Alexis lighted wound protector-retractor, flexible, large (cl303);Alexis lighted wound protector-retractor, rigid, small (cl401);Alexis lighted wound protector-retractor, rigid, medium (cl402); Alexis lighted wound protector-retractor, rigid, large (cl403)

    FDA 510(k)
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    ALEXIS LAPAROSCOPIC SYSTEM

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    ALEXIS WOUND RETRACTOR

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