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FDA 510(k)

超縫全綠延伸線

K 號:K254275 · 2026-03-23

決定日期2026-03-23
產品代碼GAT
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

HyperSuture All Green Extension Line is the device name listed in this FDA 510(k) record. The listed applicant is Threadstone, LLC. It received FDA 510(k) clearance on 2026-03-23 under 510(k) number K254275. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HyperSuture All Green Extension Line?

HyperSuture All Green Extension Line is a medical device that received FDA 510(k) clearance on 2026-03-23. The listed applicant is Threadstone, LLC. The 510(k) number is K254275.

When did HyperSuture All Green Extension Line receive FDA 510(k) clearance?

HyperSuture All Green Extension Line received FDA 510(k) clearance on 2026-03-23, under 510(k) number K254275.

Who is the listed applicant for HyperSuture All Green Extension Line?

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

What is the FDA product code for HyperSuture All Green Extension Line?

The FDA product code for HyperSuture All Green Extension Line is GAT.

相關臨床試驗

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其他以 Threadstone, LLC 為申請人之記錄

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相關器械(代碼:GAT)

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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