FDA 510(k)

藍圖雜交實境系統

K 號：K222510 · 2023-01-20

決定日期2023-01-20

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

Blueprint Mixed Reality system is the device name listed in this FDA 510(k) record. The listed applicant is Tornier S.A.S.. It received FDA 510(k) clearance on 2023-01-20 under 510(k) number K222510. 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 Blueprint Mixed Reality system?

Blueprint Mixed Reality system is a medical device that received FDA 510(k) clearance on 2023-01-20. The listed applicant is Tornier S.A.S.. The 510(k) number is K222510.

When did Blueprint Mixed Reality system receive FDA 510(k) clearance?

Blueprint Mixed Reality system received FDA 510(k) clearance on 2023-01-20, under 510(k) number K222510.

Who is the listed applicant for Blueprint Mixed Reality system?

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

What is the FDA product code for Blueprint Mixed Reality system?

The FDA product code for Blueprint Mixed Reality system is OLO.

其他以 Tornier S.A.S. 為申請人之記錄

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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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