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Petition to Ban Surgical Mesh for Transvaginal Repair of Pelvic Organ Prolapse HRG Publication 1963 Public Citizen petitions the FDA to ban the marketing of all currently available non absorbable surgical mesh products specifically designed and labeled for transvaginal repair of pelvic organ prolapse POP, order all manufacturers of these devices to recall these products and require that any non absorbable surgical mesh product specifically designed and labeled for transvaginal repair of POP that is proposed for marketing in the future be classified as a class III device and be approved for marketing only under a premarket approval application that includes data from well designed, prospective clinical trials that provide a reasonable assurance that the surgical mesh product is safe and effective <a href=http://cialis.motorcycles>buying cheap cialis online</a>

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