FDA 510(k)

E-GPS導航儀器

K 號：K220862 · 2022-07-14

決定日期2022-07-14

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

E-GPS Navigated Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Precision Spine, Inc.. It received FDA 510(k) clearance on 2022-07-14 under 510(k) number K220862. 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 E-GPS Navigated Instruments?

E-GPS Navigated Instruments is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Precision Spine, Inc.. The 510(k) number is K220862.

When did E-GPS Navigated Instruments receive FDA 510(k) clearance?

E-GPS Navigated Instruments received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220862.

Who is the listed applicant for E-GPS Navigated Instruments?

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

What is the FDA product code for E-GPS Navigated Instruments?

The FDA product code for E-GPS Navigated Instruments is OLO.

其他以 Precision Spine, Inc. 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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