簽名骨固定板系統
K 號：K241599 · 2025-02-06
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器材摘要
Signature Osteosynthesis Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Signature Orthopaedic Pty , Ltd.. It received FDA 510(k) clearance on 2025-02-06 under 510(k) number K241599. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Signature Osteosynthesis Plate System?
Signature Osteosynthesis Plate System is a medical device that received FDA 510(k) clearance on 2025-02-06. The listed applicant is Signature Orthopaedic Pty , Ltd.. The 510(k) number is K241599.
When did Signature Osteosynthesis Plate System receive FDA 510(k) clearance?
Signature Osteosynthesis Plate System received FDA 510(k) clearance on 2025-02-06, under 510(k) number K241599.
Who is the listed applicant for Signature Osteosynthesis Plate System?
The FDA 510(k) record lists Signature Orthopaedic Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Signature Osteosynthesis Plate System?
The FDA product code for Signature Osteosynthesis Plate System is HRS.
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。
相關器械（代碼：HRS）
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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