Clinical Research Details HUMANITARIAN USE DEVICE: CODMAN® ENTERPRISE Vascular Reconstruction Device and Delivery System Study Description This is for tracking an approved device composed of a new stent and a delivery system for the treatment of intracranial aneurysm. For the treatment of wide-neck, saccular or fusiform aneurysms arising from a parent vessel with a diameter of = 3 mm and = 4 mm during under fluoroscopy. Inclusion/Exclusion Criteria Inclusion: Per interventional radiologist's recommendation in cases of wide-neck, saccular or fusiform aneurysms arising from a parent vessel with a diameter of = 3 mm and = 4 mm during under fluoroscopy. Exclusion: No intracranial aneurysm. Open Enrollment Contact Name: Mauricio HernandezContact Phone: (904) 244-1257Contact Email: mauricio.hernandez@jax.ufl.edu Investigators Daniel A. Siragusa, M.D. Radiology