FDA 510(k)

動態TiBase；TRI螺釘

K 號：K241170 · 2024-10-21

決定日期2024-10-21

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Dynamic TiBase; TRI Screws 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 2024-10-21 under 510(k) number K241170. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dynamic TiBase; TRI Screws?

Dynamic TiBase; TRI Screws is a medical device that received FDA 510(k) clearance on 2024-10-21. The listed applicant is Talladium España, SL. The 510(k) number is K241170.

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

Dynamic TiBase; TRI Screws received FDA 510(k) clearance on 2024-10-21, under 510(k) number K241170.

Who is the listed applicant for Dynamic TiBase; TRI Screws?

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; TRI Screws?

The FDA product code for Dynamic TiBase; TRI Screws is NHA.

其他以 Talladium España, SL 為申請人之記錄

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相關器械（代碼：NHA）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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