An Observational Safety Evaluation of Patients Treated With the NEVO™ Sirolimus-eluting Coronary Stent. (NEVO II)
Stopped The NEVO™ stent will not be commercialized. Cordis decided to close the study after 1 years. This decision took the absence of safety signals into account.
Conditions
- Atherosclerotic Coronary Artery Disease
Interventions
- DEVICE: NEVO™ Sirolimus-eluting Coronary Stent System
- DEVICE: XIENCE V®/XIENCE PRIME™/PROMUS® Everolimus-eluting Coronary Stent System)
Sponsor
Cordis US Corp.