BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Prosthesis, Breast, Inflatable, Internal, Saline

    PMA: P990075 · Supplement: S029 · Decision Nov 26, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9

    Basic Information

    Device Name
    Prosthesis, Breast, Inflatable, Internal, Saline
    Trade Name
    MENTOR SALINE-FILLED AND SPECTRUM BREAST IMPLANT
    PMA Number
    P990075
    Supplement Number
    S029
    Device Class
    FDA Class 3
    Product Code
    FWM
    Generic Name
    Prosthesis, breast, inflatable, internal, saline
    Regulation Number
    878.3530
    Medical Specialty
    General, Plastic Surgery
    Advisory Committee
    General, Plastic Surgery
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    November 26, 2014
    Date Received
    October 27, 2014
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR MODIFICATIONS TO THE WINGED INFUSION SET ACCESSORY OF THE MENTOR SALINE-FILLED AND SPECTRUM BREAST IMPLANT. THE MODIFICATIONS INCLUDED: 1. TEXTURE, BEVELED EDGES, AND A FINGER HOLE WAS ADDED TO EACH (2) SIDE OF THE WING DESIGN; 2. PHTHALATE WAS ELIMINATED FROM THE WING MATERIAL: PVC NAKAN FEM 828 N N WITH DEHP WITH COLORANT MASTERBATCH PVC 9154 GREEN TO PVC NAKAN FEM 828 N N WITH DEHT WITH COLORANT MASTERBATCH PVC 9154 GREEN; AND3. PHTHALATE WAS ELIMINATED FROM THE TUBING MATERIAL: PVC NAKAN FMA 748 N N WITH DEHP TO PVC NAKAN FMA 748 N N WITH DEHT.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FWM Prosthesis, Breast, Inflatable, Internal, Saline