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FDA 510(k)

Tigon醫療無節結合雙針槍全縫線釘

K 號:K252596 · 2025-12-04

申請人Tigon Medical
決定日期2025-12-04
產品代碼MBI
諮詢委員會或
決定相當於

器材摘要

Tigon Medical Knotless and Dual Javelin All-Suture Anchors is the device name listed in this FDA 510(k) record. The listed applicant is Tigon Medical. It received FDA 510(k) clearance on 2025-12-04 under 510(k) number K252596. 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 Tigon Medical Knotless and Dual Javelin All-Suture Anchors?

Tigon Medical Knotless and Dual Javelin All-Suture Anchors is a medical device that received FDA 510(k) clearance on 2025-12-04. The listed applicant is Tigon Medical. The 510(k) number is K252596.

When did Tigon Medical Knotless and Dual Javelin All-Suture Anchors receive FDA 510(k) clearance?

Tigon Medical Knotless and Dual Javelin All-Suture Anchors received FDA 510(k) clearance on 2025-12-04, under 510(k) number K252596.

Who is the listed applicant for Tigon Medical Knotless and Dual Javelin All-Suture Anchors?

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

What is the FDA product code for Tigon Medical Knotless and Dual Javelin All-Suture Anchors?

The FDA product code for Tigon Medical Knotless and Dual Javelin All-Suture Anchors is MBI.

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其他以 Tigon Medical 為申請人之記錄

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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。

官方來源

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