ExacTrac 动态 (2.0); ExacTrac 动态表面
K号: K240431 · 2024-07-24
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器械摘要
常见问题
What is the ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface?
ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface is a medical device that received FDA 510(k) clearance on 2024-07-24. The listed applicant is Brainlab AG. The 510(k) number is K240431.
When did ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface receive FDA 510(k) clearance?
ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface received FDA 510(k) clearance on 2024-07-24, under 510(k) number K240431.
Who is the listed applicant for ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface?
The FDA 510(k) record lists Brainlab AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface?
The FDA product code for ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface is IYE.
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Brainlab AG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:IYE)
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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