FDA May Toughen the Regulations for Transvaginal Mesh Devices

(PRWEB) September 03, 2011 Ennis & Ennis, P.A. reports that the U.S. Food and Drug Administration (FDA) is considering regulatory changes to the classification of surgical mesh devices used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI). According to the FDA Executive Summary released yesterday, the FDA believes that ?vaginal placement of [...]

Source: http://proptomizedr.wordpress.com/2011/09/03/fda-may-toughen-the-regulations-for-transvaginal-mesh-devices/

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