Anatase 腰椎手術導航系統，型號：SNS-Spine2-S 及 SNS-spine2-V
K 號：K220348 · 2022-07-14
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器材摘要
常見問題
What is the Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?
Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Remex Medical Corporation. The 510(k) number is K220348.
When did Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V receive FDA 510(k) clearance?
Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220348.
Who is the listed applicant for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?
The FDA 510(k) record lists Remex Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?
The FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is OLO.
相關臨床試驗
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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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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