SpineUs™ 系统
K号: K241029 · 2024-10-07
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器械摘要
SpineUs™ System is the device name listed in this FDA 510(k) record. The listed applicant is Verdure Imaging. It received FDA 510(k) clearance on 2024-10-07 under 510(k) number K241029. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SpineUs™ System?
SpineUs™ System is a medical device that received FDA 510(k) clearance on 2024-10-07. The listed applicant is Verdure Imaging. The 510(k) number is K241029.
When did SpineUs™ System receive FDA 510(k) clearance?
SpineUs™ System received FDA 510(k) clearance on 2024-10-07, under 510(k) number K241029.
Who is the listed applicant for SpineUs™ System?
The FDA 510(k) record lists Verdure Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SpineUs™ System?
The FDA product code for SpineUs™ System is IYO.
相关临床试验
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相关器械（代码：IYO）
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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