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

    SU-POR SURGICAL IMPLANT

    K Number: K140437 · Decision Jun 13, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    24
    Applicant Total
    2
    Review Days
    112

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    Basic Information

    Device Name
    SU-POR SURGICAL IMPLANT
    K Number
    K140437
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.3500
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Poriferous, LLC
    Date Received
    February 21, 2014
    Decision Date
    June 13, 2014
    Product Code
    KKY
    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
    KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

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    Other Clearances by Poriferous, LLC

    K Number Device Name
    K152463 SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant