Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo Lesions
The study objective is the assessment of safety and clinical performance of Freesolve 35- and 40-mm in de novo coronary artery lesions up to 38 mm length.
Subject is ≥ 18 years and ≤ 80 years of age [+5]
Subject is hemodynamically stable with documented declining cardiac biomarkers; [+34]