FDA 510(k)

高保留附著系統

K 號：K220252 · 2022-04-14

決定日期2022-04-14

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

High Retention Attachment System is the device name listed in this FDA 510(k) record. The listed applicant is Zest Anchors, LLC. It received FDA 510(k) clearance on 2022-04-14 under 510(k) number K220252. 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 High Retention Attachment System?

High Retention Attachment System is a medical device that received FDA 510(k) clearance on 2022-04-14. The listed applicant is Zest Anchors, LLC. The 510(k) number is K220252.

When did High Retention Attachment System receive FDA 510(k) clearance?

High Retention Attachment System received FDA 510(k) clearance on 2022-04-14, under 510(k) number K220252.

Who is the listed applicant for High Retention Attachment System?

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

What is the FDA product code for High Retention Attachment System?

The FDA product code for High Retention Attachment System is NHA.

其他以 Zest Anchors, LLC 為申請人之記錄

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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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