FDA 510(k)

Sherlock

K 號：K220482 · 2022-06-21

決定日期2022-06-21

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Sherlock is the device name listed in this FDA 510(k) record. The listed applicant is Open Implants, LLC. It received FDA 510(k) clearance on 2022-06-21 under 510(k) number K220482. 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 Sherlock?

Sherlock is a medical device that received FDA 510(k) clearance on 2022-06-21. The listed applicant is Open Implants, LLC. The 510(k) number is K220482.

When did Sherlock receive FDA 510(k) clearance?

Sherlock received FDA 510(k) clearance on 2022-06-21, under 510(k) number K220482.

Who is the listed applicant for Sherlock?

The FDA 510(k) record lists Open Implants, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sherlock?

The FDA product code for Sherlock is NHA.

其他以 Open Implants, LLC 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。

K250967Sherlock K212664Sherlock K193335Sherlock

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。

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官方來源

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