FDA 510(k)

Dynamic TiBase

K号: K232151 · 2023-10-17

决定日期2023-10-17

产品代码NHA

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决定实质等同

器械摘要

Dynamic TiBase is the device name listed in this FDA 510(k) record. The listed applicant is Talladium España, SL. It received FDA 510(k) clearance on 2023-10-17 under 510(k) number K232151. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Dynamic TiBase?

Dynamic TiBase is a medical device that received FDA 510(k) clearance on 2023-10-17. The listed applicant is Talladium España, SL. The 510(k) number is K232151.

When did Dynamic TiBase receive FDA 510(k) clearance?

Dynamic TiBase received FDA 510(k) clearance on 2023-10-17, under 510(k) number K232151.

Who is the listed applicant for Dynamic TiBase?

The FDA 510(k) record lists Talladium España, SL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dynamic TiBase?

The FDA product code for Dynamic TiBase is NHA.

列明Talladium España, SL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。

K243732多单元DAS系统 K243425引导DAS手术套件 K243530Dynamic TiBase K241170Dynamic TiBase; TRI Screws K231559多单元DAS系统 K212108Dynamic TiBase

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相关器械（代码：NHA）

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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