NSite脊椎評估應用程式
K 號：K230463 · 2023-11-15
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器材摘要
NSite Scoliosis Assessment App is the device name listed in this FDA 510(k) record. The listed applicant is Nsite, Inc.. It received FDA 510(k) clearance on 2023-11-15 under 510(k) number K230463. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.
常見問題
What is the NSite Scoliosis Assessment App?
NSite Scoliosis Assessment App is a medical device that received FDA 510(k) clearance on 2023-11-15. The listed applicant is Nsite, Inc.. The 510(k) number is K230463.
When did NSite Scoliosis Assessment App receive FDA 510(k) clearance?
NSite Scoliosis Assessment App received FDA 510(k) clearance on 2023-11-15, under 510(k) number K230463.
Who is the listed applicant for NSite Scoliosis Assessment App?
The FDA 510(k) record lists Nsite, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NSite Scoliosis Assessment App?
The FDA product code for NSite Scoliosis Assessment App is LDK.
相關臨床試驗
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相關器械（代碼：LDK）
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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