Vertex 髋部骨折內固定系統
K 號：K233910 · 2024-04-04
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器材摘要
Vertex Hip Fracture Nailing System is the device name listed in this FDA 510(k) record. The listed applicant is Orthoxel Dac. It received FDA 510(k) clearance on 2024-04-04 under 510(k) number K233910. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vertex Hip Fracture Nailing System?
Vertex Hip Fracture Nailing System is a medical device that received FDA 510(k) clearance on 2024-04-04. The listed applicant is Orthoxel Dac. The 510(k) number is K233910.
When did Vertex Hip Fracture Nailing System receive FDA 510(k) clearance?
Vertex Hip Fracture Nailing System received FDA 510(k) clearance on 2024-04-04, under 510(k) number K233910.
Who is the listed applicant for Vertex Hip Fracture Nailing System?
The FDA 510(k) record lists Orthoxel Dac as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vertex Hip Fracture Nailing System?
The FDA product code for Vertex Hip Fracture Nailing System is HSB.
相關臨床試驗
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相關器械（代碼：HSB）
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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