SilverHawk 外周斑块切除术系统,TurboHawk 外周斑块切除术系统
K号: K170191 · 2017-06-16
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器械摘要
常见问题
What is the SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System?
SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System is a medical device that received FDA 510(k) clearance on 2017-06-16. The listed applicant is Medtronic Vascular, Inc.. The 510(k) number is K170191.
When did SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System receive FDA 510(k) clearance?
SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System received FDA 510(k) clearance on 2017-06-16, under 510(k) number K170191.
Who is the listed applicant for SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System?
The FDA 510(k) record lists Medtronic Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System?
The FDA product code for SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision 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。
列明Medtronic Vascular, 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。
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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