FDA Reclassifies Transvaginal Surgical Mesh Used To Repair Pelvic Organ Prolapse As High-Risk Medical Device
On January 4, 2016, the FDA announced that it was issuing two final orders regarding surgical mesh used to transvaginally repair pelvic organ prolapse (POP). One final order reclassified transvaginal surgical mesh used to repair POP from a Class II medical device (moderate-risk medical devices) [...]