Trial Comparing ELUVIA Versus Bare Metal Stent in Treatment of Superficial Femoral and/or Proximal Popliteal Artery

Inclusion Criteria: 1. Subjects age 18 and older 2. Subject is willing and able to provide consent before any study-specific test or procedure is performed, signs the consent form, and agrees to attend all required follow-up visits 3. Chronic, symptomatic lower limb ischemia defined as Rutherford categories 2, 3 or 4 4. Stenotic, restenotic or occlusive lesion(s) located in the native Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA): 1. Degree of stenosis ≥ 70 % by visual angiographic assessment 2. Vessel diameter ≥ 4 and ≤ 6 mm 3. Total lesion length (or series of lesions) ≥ 30 mm and ≤210 mm (Note: Lesion segment(s) must be fully covered with one or two overlapping ELUVIA stent(s) or Self Expanding Bare Nitinol stent(s)) 4. For occluded lesions (chronic occlusions) requiring use of re-entry device, lesion length ≤ 180 mm 5. Target lesion located at least three centimeters above the inferior edge of the femur 5. Patent infrapopliteal and popliteal artery, i.e., single vessel runoff or better with at least one of three vessels patent (\< 50 % stenosis) to the ankle or foot with no planned intervention Exclusion Criteria: 1. Previously stented target lesion/vessel 2. Target lesion/vessel previously treated with drug-coated balloon within 12 months prior to randomization/enrollment 3. Subjects who have undergone prior surgery of the SFA/PPA in the target limb to treat atherosclerotic disease 4. Use of atherectomy, laser or other debulking devices such as Rotarex in the target limb SFA/PPA during the index procedure 5. History of major amputation in the target limb 6. Documented life expectancy less than 24 months due to other medical co-morbid condition(s) that could limit the subject's ability to participate in the clinical study, limit the subject's compliance with the follow-up requirements, or impact the scientific integrity of the clinical study 7. Known hypersensitivity or contraindication to contrast dye that, in the opinion of the investigator, cannot be adequately pre-medicated 8. Known hypersensitivity/allergy to the stent system or protocol related therapies (e.g., nitinol, paclitaxel, or structurally related compounds, polymer or individual components, and antiplatelet, anticoagulant, thrombolytic medications) 9. Platelet count less than 80000 mm3 or more than 600000 mm3 or history of bleeding diathesis 10. Concomitant renal failure with a serum creatinine higher than 2.0 mg/dL 11. Receiving dialysis or immunosuppressant therapy 12. History of myocardial infarction (MI) or stroke/cerebrovascular accident (CVA) within 6 months prior to randomization/enrollment 13. Unstable angina pectoris at the time of randomization/enrollment 14. Pregnant, breast feeding, or plan to become pregnant in the next 5 years 15. Current participation in an investigational drug or device clinical study that has not completed the primary endpoint at the time of randomization/ enrollment or that clinically interferes with the current study endpoints (Note: studies requiring extended follow-up for products that were investigational, but have become commercially available since then are not considered investigational studies) 16. Septicemia at the time of randomization/enrollment 17. Presence of other hemodynamically significant outflow lesions in the target limb requiring intervention at the time of the index procedure 18. Presence of aneurysm in the target vessel 19. Acute ischemia and/or acute thrombosis of the SFA/PPA prior to randomization/enrollment 20. Perforated vessel as evidenced by extravasation of contrast media prior to randomization/enrollment 21. Heavily calcified lesions 22. As applicable by French law, subject who is a protected individual such as an incompetent adult or incarcerated person