FDA 510(k)

Argo Knotless GENESYS Anchor

K 號：K244025 · 2025-01-28

決定日期2025-01-28

產品代碼MBI

諮詢委員會或

決定相當於

器材摘要

Argo Knotless GENESYS Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2025-01-28 under 510(k) number K244025. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Argo Knotless GENESYS Anchor?

Argo Knotless GENESYS Anchor is a medical device that received FDA 510(k) clearance on 2025-01-28. The listed applicant is Conmed Corporation. The 510(k) number is K244025.

When did Argo Knotless GENESYS Anchor receive FDA 510(k) clearance?

Argo Knotless GENESYS Anchor received FDA 510(k) clearance on 2025-01-28, under 510(k) number K244025.

Who is the listed applicant for Argo Knotless GENESYS Anchor?

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

What is the FDA product code for Argo Knotless GENESYS Anchor?

The FDA product code for Argo Knotless GENESYS Anchor is MBI.

其他以 Conmed Corporation 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。

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相關器械（代碼：MBI）

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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