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FDA 510(k)

ExacTrac 动态 (2.0); ExacTrac 动态表面

K号: K240431 · 2024-07-24

申请人Brainlab AG
决定日期2024-07-24
产品代码IYE
咨询委员会RA
决定实质等同

器械摘要

ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2024-07-24 under 510(k) number K240431. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

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列明Brainlab AG为申报人的其他记录

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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。

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