FDA cleared to capture and remove embolic material produced while performing percutaneous transluminal interventional procedures in carotid arteries with reference vessel diameters of 3.5 to 7.0mm.
FDA cleared for removal of fresh, soft emboli and thrombi from vessels in the arterial system.
Volcano Announces Worldwide Exclusive Distribution Agreement With Lumen Biomedical for Xtract(TM) Thrombus Aspiration Catheter
Invatec Announces Worldwide Distribution Agreement with Lumen Biomedical
FDA Approves Lumen Biomedical’s FiberNet Embolic Protection System for Carotid Artery Stenting
Lumen Biomedical Receives FDA Clearance of Embolectomy System for Treatment of Peripheral Artery Disease
FiberNet EPS Clinical Trial Results
Lumen Presence at TCT Conference
Fibernet® Embolic Protection System, Exploring the Differences. Featured Technology, Endovascular Today
