Clinical Research Directory

Inclusion Criteria: 1. Any subject with below the knee, at the ankle level or below the ankle peripheral arterial lesions previously treated or intended to be treated with the MicroStent® System per the current indications for use 2. For across the ankle joint intervention, distal runoff to digital branches or arcuate arteries must be present on angiography prior to MicroStent deployment 3. Subject's age is ≥ 18 years. 4. Subject must be willing to sign a patient informed consent form. Exclusion Criteria: 1. Subject is pregnant or planning to become pregnant during the study duration 2. Subject has a life expectancy of less than one (1) year 3. Subject has a known allergy to concomitant medication, contrast agents (that cannot be medically managed), anti-platelet, anti-coagulant or thrombolytic medications 4. Subject is enrolled in another study that has not reached its primary endpoint at the time of enrollment.