P090003 Express® LD Iliac Premounted Stent System

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Date: 2013-12-06 12:12:06 Health Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Investigational Device Exemption Food and Drug Administration Medicine Technology		P090003 Express® LD Iliac Premounted Stent System Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 167,06 KB Share Document on Facebook

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