FDA 510(k)

脊椎計劃（2.0版），Elements脊椎計劃，Elements計劃脊椎

K 號：K223553 · 2023-08-02

決定日期2023-08-02

產品代碼OLO

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

Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2023-08-02 under 510(k) number K223553. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine?

Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine is a medical device that received FDA 510(k) clearance on 2023-08-02. The listed applicant is Brainlab AG. The 510(k) number is K223553.

When did Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine receive FDA 510(k) clearance?

Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine received FDA 510(k) clearance on 2023-08-02, under 510(k) number K223553.

Who is the listed applicant for Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine?

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 Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine?

The FDA product code for Spine Planning (2.0), Elements Spine Planning, Elements Planning Spine is OLO.

其他以 Brainlab AG 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。

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相關器械（代碼：OLO）

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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