Vortex5 尾骨矫正系统
K号: K260291 · 2026-03-25
广告
器械摘要
常见问题
What is the Vortex5 Tailor's Bunion Correction System?
Vortex5 Tailor's Bunion Correction System is a medical device that received FDA 510(k) clearance on 2026-03-25. The listed applicant is Nvision Biomedical Technologies, Inc.. The 510(k) number is K260291.
When did Vortex5 Tailor's Bunion Correction System receive FDA 510(k) clearance?
Vortex5 Tailor's Bunion Correction System received FDA 510(k) clearance on 2026-03-25, under 510(k) number K260291.
Who is the listed applicant for Vortex5 Tailor's Bunion Correction System?
The FDA 510(k) record lists Nvision Biomedical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vortex5 Tailor's Bunion Correction System?
The FDA product code for Vortex5 Tailor's Bunion Correction System is HRS.
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, 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:HRS)
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。
广告