刺激器，骨生長，非侵入式
PMA 核准號：P850007 · 2022-06-14
廣告
器材摘要
Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Orthofix, Inc.. It received FDA 510(k) clearance on 2022-06-14. The device is classified under product code LOF. It was reviewed by the OR advisory panel.
常見問題
What is the Stimulator, bone growth, non-invasive?
Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2022-06-14. The listed applicant is Orthofix, Inc..
When did Stimulator, bone growth, non-invasive receive FDA 510(k) clearance?
The clearance date for Stimulator, bone growth, non-invasive can be found in the official FDA records.
Who is the listed applicant for Stimulator, bone growth, non-invasive?
The FDA 510(k) record lists Orthofix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, bone growth, non-invasive?
The FDA product code for Stimulator, bone growth, non-invasive is LOF.
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。
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