植入式，可吸收，用於關節軟骨修復
PMA 核准號：P210034 · 2026-06-04
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器材摘要
Implant, resorbable, for articular osteochondral repair is the device name listed in this FDA 510(k) record. The listed applicant is Smith and Nephew, Inc.. It received FDA 510(k) clearance on 2026-06-04. The device is classified under product code QRU. It was reviewed by the OR advisory panel.
常見問題
What is the Implant, resorbable, for articular osteochondral repair?
Implant, resorbable, for articular osteochondral repair is a medical device that received FDA 510(k) clearance on 2026-06-04. The listed applicant is Smith and Nephew, Inc..
When did Implant, resorbable, for articular osteochondral repair receive FDA 510(k) clearance?
The clearance date for Implant, resorbable, for articular osteochondral repair can be found in the official FDA records.
Who is the listed applicant for Implant, resorbable, for articular osteochondral repair?
The FDA 510(k) record lists Smith and Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implant, resorbable, for articular osteochondral repair?
The FDA product code for Implant, resorbable, for articular osteochondral repair is QRU.
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。
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