SISTEMA DE FIJACIÓN ESPINAL VIRAGE OCT
EL SISTEMA DE FIJACIÓN ESPINAL, ESTÁ DISEÑADO PARA PROMOVER LA FUSIÓN DE LA COLUMNA OCCIPITO-CERVICAL, CERVICAL Y TORÁCICA (OCCIPUCIO-T3) EN PACIENTES CON ENFERMEDAD DEGENERATIVA DE DISCO (DDD), ESPONDILOLISTESIS, ESTENOSIS ESPINAL, FRACTURA, DISLOCACIÓN,
THE SPINAL FIXATION SYSTEM IS DESIGNED TO PROMOTE FUSION OF THE OCCIPITO-CERVICAL, CERVICAL AND THORACIC SPINE (OCCIPUT-T3) IN PATIENTS WITH DEGENERATIVE DISC DISEASE (DDD), SPONDYLOLISTHESIS, SPINAL STENOSIS, FRACTURE, DISLOCATION,
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- SISTEMA PARA FIJACIÓN ESPINAL NO CERVICAL
- Trade Name (English)
- NON-CERVICAL SPINAL FIXATION SYSTEM
- Analysis ID
- 1894C2019 SSA
- Registration Date
- September 24, 2019
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for SISTEMA DE FIJACIÓN ESPINAL VIRAGE OCT (VIRAGE OCT SPINAL FIXATION SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1894C2019 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on September 24, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.