FDA 510(k)

NEOVIEW 鍍膜系統

K 號：K160995 · 2016-06-10

決定日期2016-06-10

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

NEOVIEW Plating System is the device name listed in this FDA 510(k) record. The listed applicant is In2bones Sas. It received FDA 510(k) clearance on 2016-06-10 under 510(k) number K160995. 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 NEOVIEW Plating System?

NEOVIEW Plating System is a medical device that received FDA 510(k) clearance on 2016-06-10. The listed applicant is In2bones Sas. The 510(k) number is K160995.

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

NEOVIEW Plating System received FDA 510(k) clearance on 2016-06-10, under 510(k) number K160995.

Who is the listed applicant for NEOVIEW Plating System?

The FDA 510(k) record lists In2bones Sas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEOVIEW Plating System?

The FDA product code for NEOVIEW Plating System is HRS.

其他以 In2bones Sas 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。

K231699QUANTUM® 病患特定儀器設備（PSI）系統 K230313量子病人特定儀器設備（PSI）系統 K211883QUANTUM® 病患特定儀器設備（PSI）系統 K191380量子® 全踝人工關節 K173811TRIWAY 膝踝跟骨融合系統 (TTC)K173616DIP關節融合系統

查看所有 14 項裝置 →

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

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。