FDA 510(k)

橋梁支撐

K 號：K153779 · 2016-03-31

決定日期2016-03-31

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Abutment for Bridges is the device name listed in this FDA 510(k) record. The listed applicant is Altatec GmbH. It received FDA 510(k) clearance on 2016-03-31 under 510(k) number K153779. 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 Abutment for Bridges?

Abutment for Bridges is a medical device that received FDA 510(k) clearance on 2016-03-31. The listed applicant is Altatec GmbH. The 510(k) number is K153779.

When did Abutment for Bridges receive FDA 510(k) clearance?

Abutment for Bridges received FDA 510(k) clearance on 2016-03-31, under 510(k) number K153779.

Who is the listed applicant for Abutment for Bridges?

The FDA 510(k) record lists Altatec GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Abutment for Bridges?

The FDA product code for Abutment for Bridges is NHA.

其他以 Altatec GmbH 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。

K193401Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants K160784CAM钛材空白 K152509CAMLOG及CONELOG螺釘固定修復體基座（ASR）

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。

K262207固定式加長基座Unidental Co., Ltd.K260940貝拉特克條ZimVie US Corp, LLC K253999通用基座 ASC 接合；通用基座 ASC 非接合；通用基座 MUA ASC；臨時基座接合和非接合；恢復基座極锥連接；Omnigrip臨床螺釘鈦金；Omnigrip假牙螺釘Nobel Biocare AB K261147Neodent植牙系統 - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLC K260061生物地平線 CEREC 兼容 Ti-BasesBioHorizons Implant Systems, Inc.

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。