Safety and Efficacy of the SurVeil™ Drug-Coated Balloon

Inclusion Criteria

• Subject is ≥18 years.
• Subject has target limb Rutherford classification 2, 3 or 4.
• Subject has provided written informed consent and is willing to comply with study follow-up requirements.
• De novo lesion(s) or non-stented restenotic lesion(s) occurring >90 days after prior plain old balloon (POBA) angioplasty or >180 days after prior DCB treatment.
• Target lesion location starts ≥10 mm below the common femoral bifurcation and terminates distally at or above the end of the P1 segment of the popliteal artery.
• Target vessel diameter ≥4 mm and ≤7 mm.
• Target lesion must have angiographic evidence of ≥70% stenosis by operator visual estimate.
• Chronic total occlusions may be included only after successful, uncomplicated wire crossing of target lesion via an anterograde approach and without the use of subintimal dissection techniques.
• Target lesion must be ≤180 mm in length (one long lesion or multiple serial lesions) by operator visual estimate. Note: combination lesions must have a total lesion length of ≤180 mm by visual estimate and be separated by ≤30 mm.
• Target lesion is located at least 30 mm from any stent, if target vessel was previously stented.
• Successful, uncomplicated (without use of a crossing device) wire crossing of target lesion. Successful crossing of the target lesion occurs when the tip of the guide wire is distal to the target lesion without the occurrence of flow-limiting dissection or perforation and is judged by visual inspection to be within the true lumen.
• After pre-dilatation, the target lesion is ≤70% residual stenosis, absence of a flow limiting dissection and treatable with available device matrix.
• A patent inflow artery free from significant stenosis (≥50% stenosis) as confirmed by angiography.
• At least one patent native outflow artery to the ankle or foot, free from significant stenosis (≥50% stenosis) as confirmed by angiography.

Exclusion Criteria

• Subject has acute limb ischemia.
• Subject underwent percutaneous transluminal angioplasty (PTA) of the target limb using plain old balloon angioplasty (POBA) or a stent within the previous 90 days.
• Subject underwent any lower extremity percutaneous treatment using a paclitaxel-eluting stent or a DCB within the previous 90 days.
• Subject underwent PTA of the target lesion using a DCB within the previous 180 days.
• Subject has had prior vascular intervention in the contralateral limb within 14 days before the planned study index procedure or subject has planned vascular intervention in the contralateral limb within 30 days after the index procedure.
• Subject is pregnant, breast-feeding or intends to become pregnant during the time of the study.
• Subject has life expectancy less than 2 years.
• Subject has a known allergy to contrast medium that cannot be adequately pre-medicated.
• Subject is allergic to ALL antiplatelet treatments.
• Subject has impaired renal function (i.e. serum creatinine level ≥2.5 mg/dL).
• Subject is dialysis dependent.
• Subject is receiving immunosuppressant therapy.
• Subject has known or suspected active infection at the time of the index procedure.
• Subject has platelet count 700,000/mm3.
• Subject has history of gastrointestinal hemorrhage requiring a transfusion within 3 months prior to the study procedure.
• Subject is diagnosed with coagulopathy that precludes treatment with systemic anticoagulation and/or dual antiplatelet therapy (DAPT).
• Subject has history of stroke within the past 90 days.
• Subject has a history of myocardial infarction within the past 30 days.
• Subject is unable to tolerate blood transfusions because of religious beliefs or other reasons.
• Subject is incarcerated, mentally incompetent, or abusing drugs or alcohol.
• Subject is participating in another investigational drug or medical device study that has not completed primary endpoint(s) evaluation or that clinically interferes with the endpoints from this study, or subject is planning to pa