動力脊柱
K 號：K232023 · 2023-10-04
廣告
器材摘要
Momentum Spine is the device name listed in this FDA 510(k) record. The listed applicant is Momentum Health, Inc.. It received FDA 510(k) clearance on 2023-10-04 under 510(k) number K232023. The device is classified under product code LDK. FDA Decision: Substantially Equivalent.
常見問題
What is the Momentum Spine?
Momentum Spine is a medical device that received FDA 510(k) clearance on 2023-10-04. The listed applicant is Momentum Health, Inc.. The 510(k) number is K232023.
When did Momentum Spine receive FDA 510(k) clearance?
Momentum Spine received FDA 510(k) clearance on 2023-10-04, under 510(k) number K232023.
Who is the listed applicant for Momentum Spine?
The FDA 510(k) record lists Momentum Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Momentum Spine?
The FDA product code for Momentum Spine is LDK.
相關臨床試驗
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。
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。
廣告