FDA 510(k)

GMReis 靈骨板系統

K 號：K242998 · 2024-11-21

申請人GM Dos Reis Industria e Comercio Ltda.

決定日期2024-11-21

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

GMReis Ankle Plating System 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 2024-11-21 under 510(k) number K242998. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the GMReis Ankle Plating System?

GMReis Ankle Plating System is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is GM Dos Reis Industria e Comercio Ltda.. The 510(k) number is K242998.

When did GMReis Ankle Plating System receive FDA 510(k) clearance?

GMReis Ankle Plating System received FDA 510(k) clearance on 2024-11-21, under 510(k) number K242998.

Who is the listed applicant for GMReis Ankle Plating System?

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 GMReis Ankle Plating System?

The FDA product code for GMReis Ankle Plating System is HRS.

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。

K253910釘線 - 緝合針線及膠帶 K262537Versalock 無菌板片系統 K261406Versalock Proximal Tibial Plating System K260390超上肢 Versalock 鋼板系統 K254188半月板Versaflex K252664GMReis 緝合釘

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相關器械（代碼：HRS）

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。

K261892ProRib固定系統Costa Surgical, Inc.K262098EnHAnce PEEK 趾骨隆起系統Nvision Biomedical Technologies K262963TMC 偽骨固定系統Treace Medical Concepts, Inc.K261647Tempo植板系統；超壓縮螺釘系統Pace Surgical K261830FRAXION 3.5 板系統（多種 - 見目錄）；FRAXION 4.5 板系統（多種 - 見目錄）；FRAXION Mini 板系統（多種 - 見目錄）；FRAXION 骨釘系統（多種 - 見目錄）Ortler Global Tibbi Gerecler Anonim Sirketi K262537Versalock 無菌板片系統GM Dos Reis Industria e Comercio Ltda.

官方來源

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