刺激器，骨生長，非侵入式
PMA 核准號：P900009 · 2026-03-06
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 Bioventus, LLC. It received FDA 510(k) clearance on 2026-03-06. 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 2026-03-06. The listed applicant is Bioventus, LLC.
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?
FDA 510(k) 記錄將 Bioventus, LLC 列為申請人。這並不單獨確立設備製造商。
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
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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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