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FDA 510(k)

ViperWire高级导丝，Stealth 360轨道外周动脉粥样硬化切除术装置（PAD），DIAMONDBACK 360外周动脉粥样硬化切除术系统

K号: K180416 · 2018-04-17

申请人Cardiovascular Systems, Inc.
决定日期2018-04-17
产品代码MCW
咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同

器械摘要

ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Cardiovascular Systems, Inc.. It received FDA 510(k) clearance on 2018-04-17 under 510(k) number K180416. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System?

ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System is a medical device that received FDA 510(k) clearance on 2018-04-17. The listed applicant is Cardiovascular Systems, Inc.. The 510(k) number is K180416.

When did ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System receive FDA 510(k) clearance?

ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System received FDA 510(k) clearance on 2018-04-17, under 510(k) number K180416.

Who is the listed applicant for ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System?

The FDA 510(k) record lists Cardiovascular Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System?

The FDA product code for ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System is MCW.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Cardiovascular Systems, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K220109DIAMONDBACK 360 外周轨道血管成形术系统，DIAMONDBACK 360 外周轨道血管成形术系统，可交换系列，Stealth 360 外周轨道血管成形术系统K212725ViperCross 支撑导丝导管K210586Diamonback 360 外周轨道动脉粥样硬化系统，Diamondback 360 隐形轨道动脉粥样硬化系统K211240ViperCross 支撑导丝导管K211251ViperCath XC 外周交换导管K210282WIRION 颗粒保护系统

查看所有 13 个设备 →

相关器械（代码：MCW）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K260244Auryon 激光旋切系统Eximo MedicalK250723FreedomFlow®轨道环形动脉粥样硬化系统（H6005/ 4Fr 3球配置）Cardio Flow Inc.,K250385Turbo-Elite 激光动脉粥样硬化切除术导管SpectraneticsK242757Rotarex 激光消融系统Bard Peripheral Vascular, Inc.K242947FreedomFlow®轨道环形动脉粥样硬化系统Cardio Flow Inc.,K241553Auryon 搔刮导管 1.7mm；Auryon 搔刮导管 1.7mm，亲水涂层Eximo Medical, Ltd.

官方来源

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