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FDA 510(k)

Tigon醫療靜態飛鏢全縫線固定針及飛鏢全縫線固定針系列

K 號:K260921 · 2026-04-21

申請人Tigon Medical
決定日期2026-04-21
產品代碼MBI
諮詢委員會或
決定相當於

器材摘要

Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line is the device name listed in this FDA 510(k) record. The listed applicant is Tigon Medical. It received FDA 510(k) clearance on 2026-04-21 under 510(k) number K260921. 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 Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line?

Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line is a medical device that received FDA 510(k) clearance on 2026-04-21. The listed applicant is Tigon Medical. The 510(k) number is K260921.

When did Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line receive FDA 510(k) clearance?

Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line received FDA 510(k) clearance on 2026-04-21, under 510(k) number K260921.

Who is the listed applicant for Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line?

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 Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line?

The FDA product code for Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line is MBI.

相關臨床試驗

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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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