Articulator 間鏡刀
K 號：K252666 · 2025-11-21
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器材摘要
Articulator Arthroscopic Bur is the device name listed in this FDA 510(k) record. The listed applicant is Joint Preservation Innovations, LLC. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K252666. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Articulator Arthroscopic Bur?
Articulator Arthroscopic Bur is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Joint Preservation Innovations, LLC. The 510(k) number is K252666.
When did Articulator Arthroscopic Bur receive FDA 510(k) clearance?
Articulator Arthroscopic Bur received FDA 510(k) clearance on 2025-11-21, under 510(k) number K252666.
Who is the listed applicant for Articulator Arthroscopic Bur?
The FDA 510(k) record lists Joint Preservation Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Articulator Arthroscopic Bur?
The FDA product code for Articulator Arthroscopic Bur is HRX.
相關臨床試驗
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相關器械（代碼：HRX）
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。
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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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