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SYNERGY Stent Investigator-Sponsored Research

October 12, 2015

Boston Scientific is not responsible for the collection, analysis or reporting of the investigator-sponsored research output which is the sole responsibility of the investigators. Boston Scientific’s involvement in investigator-sponsored research is limited to providing financial support for research that advances medical and scientific knowledge about our products. Safety and performance of the SYNERGY Coronary Stent System has not been established for use in patients with STEMI, chronic total occlusion, bifurcation, left main disease, and multi-vessel disease stenting. The SYNERGY Stent System is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease due to discrete de novo native coronary artery lesions. CE Mark Approved 2012.

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