Vector锤状趾矫正系统
K号: K183055 · 2019-02-19
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器械摘要
常见问题
What is the Vector Hammertoe Correction System?
Vector Hammertoe Correction System is a medical device that received FDA 510(k) clearance on 2019-02-19. The listed applicant is Nvision Biomedical Technologies, LLC. The 510(k) number is K183055.
When did Vector Hammertoe Correction System receive FDA 510(k) clearance?
Vector Hammertoe Correction System received FDA 510(k) clearance on 2019-02-19, under 510(k) number K183055.
Who is the listed applicant for Vector Hammertoe Correction System?
The FDA 510(k) record lists Nvision Biomedical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vector Hammertoe Correction System?
The FDA product code for Vector Hammertoe Correction System is HWC. This falls under the Cardiovascular category.
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Nvision Biomedical Technologies, LLC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:HWC)
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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