FDA 510(k)

CONMED 阿爾戈 Knotless® 抓釘

K 號：K251530 · 2025-06-18

決定日期2025-06-18

產品代碼MBI

諮詢委員會或

決定相當於

器材摘要

CONMED Argo Knotless® 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 2025-06-18 under 510(k) number K251530. 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 CONMED Argo Knotless® Anchor?

CONMED Argo Knotless® Anchor is a medical device that received FDA 510(k) clearance on 2025-06-18. The listed applicant is Conmed Corporation. The 510(k) number is K251530.

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

CONMED Argo Knotless® Anchor received FDA 510(k) clearance on 2025-06-18, under 510(k) number K251530.

Who is the listed applicant for CONMED Argo Knotless® 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 CONMED Argo Knotless® Anchor?

The FDA product code for CONMED Argo Knotless® 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。

K261363Y-Knotless™ 非結節式靈活釘 K253763Y-Knotless™ 非結節式靈活釘 K252946BioBrace® 間節韌帶增強組合 K250395BioBrace® RC 交付系統 K244025Argo Knotless GENESYS Anchor K242187BioBrace®

查看所有 47 項裝置 →

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。

K261869整潔式可收回式植入器插入器（6000127）Anika Therapeutics, Inc.K253065Aevumed SUPERCYNCH™按鈕系統Aevumed, Inc.K262809ArthroTAK 軟骨組織锚定組合包ArthroTAK, LLC K262677Iconix Knotless TRiverpoint Medical K262047Grappler縫合釘系統Paragon 28, Inc.K262369AIR+ 全內側半月板修復設備，向上曲；AIR+ 全內側半月板修復設備，向下曲Stryker Endoscopy

官方來源

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