關節，颚關節，植入物
PMA 核准號：P980052 · 2026-03-06
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決定日期2026-03-06
PMA 編號P980052
產品代碼LZD
器械分類3 類
醫療專科D
法規編號21 CFR 8
諮詢委員會DE
器材摘要
Joint, temporomandibular, implant is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger, GmbH & Co KG. It received FDA 510(k) clearance on 2026-03-06. The device is classified under product code LZD. It was reviewed by the DE advisory panel.
常見問題
What is the Joint, temporomandibular, implant?
Joint, temporomandibular, implant is a medical device that received FDA 510(k) clearance on 2026-03-06. The listed applicant is Stryker Leibinger, GmbH & Co KG.
When did Joint, temporomandibular, implant receive FDA 510(k) clearance?
The clearance date for Joint, temporomandibular, implant can be found in the official FDA records.
Who is the listed applicant for Joint, temporomandibular, implant?
The FDA 510(k) record lists Stryker Leibinger, GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Joint, temporomandibular, implant?
The FDA product code for Joint, temporomandibular, implant is LZD.
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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