脊椎網絡SSP系統
K 號：K200170 · 2020-02-05
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器材摘要
SpineNet SSP System is the device name listed in this FDA 510(k) record. The listed applicant is Spinenet, LLC. It received FDA 510(k) clearance on 2020-02-05 under 510(k) number K200170. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SpineNet SSP System?
SpineNet SSP System is a medical device that received FDA 510(k) clearance on 2020-02-05. The listed applicant is Spinenet, LLC. The 510(k) number is K200170.
When did SpineNet SSP System receive FDA 510(k) clearance?
SpineNet SSP System received FDA 510(k) clearance on 2020-02-05, under 510(k) number K200170.
Who is the listed applicant for SpineNet SSP System?
The FDA 510(k) record lists Spinenet, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SpineNet SSP System?
The FDA product code for SpineNet SSP System is KWQ.
相關臨床試驗
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相關器械（代碼：KWQ）
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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