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FDA 510(k)

Trigon Trigon HA 独立楔形固定系統

K 號:K234116 · 2024-01-26

決定日期2024-01-26
產品代碼PLF
諮詢委員會或
決定相當於

器材摘要

Trigon Trigon HA Stand-Alone Wedge Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Nvision Biomedical Technologies. It received FDA 510(k) clearance on 2024-01-26 under 510(k) number K234116. The device is classified under product code PLF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Trigon Trigon HA Stand-Alone Wedge Fixation System?

Trigon Trigon HA Stand-Alone Wedge Fixation System is a medical device that received FDA 510(k) clearance on 2024-01-26. The listed applicant is Nvision Biomedical Technologies. The 510(k) number is K234116.

When did Trigon Trigon HA Stand-Alone Wedge Fixation System receive FDA 510(k) clearance?

Trigon Trigon HA Stand-Alone Wedge Fixation System received FDA 510(k) clearance on 2024-01-26, under 510(k) number K234116.

Who is the listed applicant for Trigon Trigon HA Stand-Alone Wedge Fixation System?

FDA 510(k) 記錄將 Nvision Biomedical Technologies 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Trigon Trigon HA Stand-Alone Wedge Fixation System?

The FDA product code for Trigon Trigon HA Stand-Alone Wedge Fixation System is PLF.

相關臨床試驗

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。

其他以 Nvision Biomedical Technologies 為申請人之記錄

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。

相關器械(代碼:PLF)

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。

官方來源

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