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FDA 510(k)

Navient影像導航系統(955-NC-NC),頭部

K 號:K241327 · 2025-02-05

申請人Claronav
決定日期2025-02-05
產品代碼HAW
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Navient Image Guide Navigation System (955-NC-NC), Cranial is the device name listed in this FDA 510(k) record. The listed applicant is Claronav. It received FDA 510(k) clearance on 2025-02-05 under 510(k) number K241327. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Navient Image Guide Navigation System (955-NC-NC), Cranial?

Navient Image Guide Navigation System (955-NC-NC), Cranial is a medical device that received FDA 510(k) clearance on 2025-02-05. The listed applicant is Claronav. The 510(k) number is K241327.

When did Navient Image Guide Navigation System (955-NC-NC), Cranial receive FDA 510(k) clearance?

Navient Image Guide Navigation System (955-NC-NC), Cranial received FDA 510(k) clearance on 2025-02-05, under 510(k) number K241327.

Who is the listed applicant for Navient Image Guide Navigation System (955-NC-NC), Cranial?

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

What is the FDA product code for Navient Image Guide Navigation System (955-NC-NC), Cranial?

The FDA product code for Navient Image Guide Navigation System (955-NC-NC), Cranial is HAW.

相關臨床試驗

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其他以 Claronav 為申請人之記錄

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相關器械(代碼:HAW)

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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