MRI 兼容現有 BioHorizons 牙齒植體及基座
K 號:K223697 · 2023-10-13
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器材摘要
常見問題
What is the MRI compatibility for existing BioHorizons dental implants and abutments?
MRI compatibility for existing BioHorizons dental implants and abutments is a medical device that received FDA 510(k) clearance on 2023-10-13. The listed applicant is BioHorizons Implant Systems, Inc.. The 510(k) number is K223697.
When did MRI compatibility for existing BioHorizons dental implants and abutments receive FDA 510(k) clearance?
MRI compatibility for existing BioHorizons dental implants and abutments received FDA 510(k) clearance on 2023-10-13, under 510(k) number K223697.
Who is the listed applicant for MRI compatibility for existing BioHorizons dental implants and abutments?
The FDA 510(k) record lists BioHorizons Implant Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRI compatibility for existing BioHorizons dental implants and abutments?
The FDA product code for MRI compatibility for existing BioHorizons dental implants and abutments is DZE.
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。
其他以 BioHorizons Implant Systems, Inc. 為申請人之記錄
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:DZE)
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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