NMT STARFlex Single-Arm Study Insufficient For Approval, Panel Concludes

NMT Medical must conduct a randomized controlled trial of the STARFlex septal occlusion system to demonstrate that the device is superior to medical therapy in preventing strokes, FDA's Circulatory System Devices Panel concluded at its Sept. 10 meeting in Gaithersburg, Maryland

More from Archive

More from Medtech Insight