DevicePMAs@therightstef:P110040_S000 / 281-290
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Approval for the medtronic vascular complete se vascular stent system. this device is indicated to improve luminal diameter in symptomatic patients with de novo and/or restenotic lesions or occlusions of the superficial femoral artery (sfa) or proximal popliteal artery (ppa) with reference diameters ranging from 4 mm to 7 mm and lesion lengths up to 140 mm.
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