In Brief: FDA Gastroenterology and Urology Devices Panel
This article was originally published in The Gray Sheet
Executive Summary
FDA Gastroenterology and Urology Devices Panel: Slated to meet Jan. 16 in Rockville, Maryland to discuss a premarket approval application for "a metallic mesh stent intended to relieve benign prostatic hyperplasia or bladder neck contracture." An FDA presentation on a draft guidance for penile rigidity implants also is on the agenda. For more information, contact Mary J. Cornelius at 301/594-2194...