FDA 510(k)

KLOCKNER 齒齒植體基座（II）

K 號：K151194 · 2016-01-29

決定日期2016-01-29

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is the device name listed in this FDA 510(k) record. The listed applicant is SOADCO, S.L.. It received FDA 510(k) clearance on 2016-01-29 under 510(k) number K151194. 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 KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is a medical device that received FDA 510(k) clearance on 2016-01-29. The listed applicant is SOADCO, S.L.. The 510(k) number is K151194.

When did KLOCKNER DENTAL IMPLANT ABUTMENTS (II) receive FDA 510(k) clearance?

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) received FDA 510(k) clearance on 2016-01-29, under 510(k) number K151194.

Who is the listed applicant for KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

The FDA 510(k) record lists SOADCO, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

The FDA product code for KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is NHA.

其他以 SOADCO, S.L. 為申請人之記錄

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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

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