免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

諾貝爾普雷塞拉钛金 ASC 牙根擴張器,奧米格里普臨床螺釘 钛金

K 號:K233208 · 2024-01-24

決定日期2024-01-24
產品代碼NHA
諮詢委員會DE
決定相當於

器材摘要

NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare AB. It received FDA 510(k) clearance on 2024-01-24 under 510(k) number K233208. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium?

NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium is a medical device that received FDA 510(k) clearance on 2024-01-24. The listed applicant is Nobel Biocare AB. The 510(k) number is K233208.

When did NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium receive FDA 510(k) clearance?

NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium received FDA 510(k) clearance on 2024-01-24, under 510(k) number K233208.

Who is the listed applicant for NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium?

FDA 510(k) 記錄將 Nobel Biocare AB 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium?

The FDA product code for NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium is NHA.

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 Nobel Biocare AB 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。

查看所有 41 項裝置 →

相關器械(代碼:NHA)

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。

↑