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2011年美国食品药品监督管理局医疗器械咨询委员会会议中关于Zilver® PTX®药物洗脱外周支架的循环系统器械小组会议概述

Overview of the 2011 food and drug administration's circulatory system devices panel of the medical devices advisory committee meeting on the Zilver® PTX® drug-eluting peripheral stent.

作者信息

Dvir Danny, Torguson Rebecca, Waksman Ron

机构信息

Interventional Cardiology, Washington Hospital Center, Washington, DC 20010, USA.

出版信息

Cardiovasc Revasc Med. 2012 Sep-Oct;13(5):281-5. doi: 10.1016/j.carrev.2012.05.003. Epub 2012 Aug 14.

Abstract

Zilver® PTX® (Cook Medical, Bloomington, IN) is a self-expanding nitinol drug-eluting stent with a polymer-free paclitaxel coating on its outer surface. The stent aims to provide improved treatment for patients with symptomatic peripheral arterial disease in the above-the-knee femoropopliteal arteries. On October 13, 2011, the Food and Drug Administration's (FDA) Circulatory System Devices Panel reviewed the Zilver PTX premarket approval application. This summary aims to describe the discussions and recommendations made during the meeting. Based on the Panel's recommendations, it is anticipated that the device will be approved by the FDA.

摘要

Zilver® PTX®(库克医疗公司,印第安纳州布卢明顿)是一种自膨胀镍钛诺药物洗脱支架,其外表面涂有无聚合物紫杉醇涂层。该支架旨在为患有症状性股腘动脉疾病的患者提供更好的治疗。2011年10月13日,美国食品药品监督管理局(FDA)循环系统设备小组审查了Zilver PTX的上市前批准申请。本摘要旨在描述会议期间的讨论和建议。根据小组的建议,预计该设备将获得FDA的批准。

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