FDA 510(k)

半月板Versaflex

K 號：K254188 · 2026-02-19

申請人GM Dos Reis Industria e Comercio Ltda.

決定日期2026-02-19

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

Meniscus Versaflex is the device name listed in this FDA 510(k) record. The listed applicant is GM Dos Reis Industria e Comercio Ltda.. It received FDA 510(k) clearance on 2026-02-19 under 510(k) number K254188. 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 Meniscus Versaflex?

Meniscus Versaflex is a medical device that received FDA 510(k) clearance on 2026-02-19. The listed applicant is GM Dos Reis Industria e Comercio Ltda.. The 510(k) number is K254188.

When did Meniscus Versaflex receive FDA 510(k) clearance?

Meniscus Versaflex received FDA 510(k) clearance on 2026-02-19, under 510(k) number K254188.

Who is the listed applicant for Meniscus Versaflex?

FDA 510(k) 記錄將 GM Dos Reis Industria e Comercio Ltda. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Meniscus Versaflex?

The FDA product code for Meniscus Versaflex is GAT.

其他以 GM Dos Reis Industria e Comercio Ltda. 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：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。

K253910釘線 - 緝合針線及膠帶GM Dos Reis Industria e Comercio Ltda.K261021EasyWhip 家族Winter Innovations, Inc.K260775聚乙烯；聚乙烯融合；聚乙烯正骨膠帶™Teleflex Medical, LLC K254275超縫全綠延伸線Threadstone, LLC K253145預縫合腱Rti Surgical, Inc.K253024ProZip 齊結式植入體Riverpoint Medical

官方來源

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