INSTRUMENTAL PARA SISTEMA DE TORNILLO FACETARIO CONCERO® - COFEPRIS Registration 1197E2019 SSA
Access comprehensive regulatory information for INSTRUMENTAL PARA SISTEMA DE TORNILLO FACETARIO CONCERO® (INSTRUMENTATION FOR FACET SCREW SYSTEM CONCERO®) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1197E2019 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on May 31, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
EL INSTRUMENTAL PARA SISTEMA DE TORNILLO FACETARIO CONCERO® ESTÁ DISEÑADO PARA LA IMPLANTACIÓN DEL SISTEMA CONCERO® QUE PROMUEVE LA FUSIÓN DE LA COLUMNA VERTEBRAL (C2-S1) EN PACIENTES CON PSEUDOARTROSIS, FUSIÓN PREVIA FALLIDA SINTOMÁTICA, QUE PUEDA CAUSA
THE INSTRUMENTS FOR CONCERO FACET SCREW SYSTEM ARE DESIGNED FOR THE IMPLANTATION OF THE CONCERO®® SYSTEM THAT PROMOTES FUSION OF THE SPINE (C2-S1) IN PATIENTS WITH PSEUDOARTHROSIS, PREVIOUS SYMPTOMATIC FAILED FUSION, WHICH MAY CAUSE