DevicePMAs@therightstef:P000018_S028 / 0-8
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Approval for the 60 mm beta-cath 3.5f system. The device, as modified, is indicated to deliver beta radiation to the site of successful percutaneous coronary intervention (pci) for the treatment of in-stent restenosis in native coronary arteries with discrete lesions (treatable with a 20 mm balloon for the 30 mm and 40 mm systems and injury areas up to 40 mm for the 60 mm system) in a reference vessel diameter ranging from 2.7 mm to 4.0 mm.
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projects
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