Pure Global

CORNERSTONE ® PSR CERVICAL FUSION SYSTEM-SISTEMA DE FUSION CERVICAL CORNESTONE® - INVIMA Registration d5b108dcec6eafbfa9715f6bd8069f7f

Access comprehensive regulatory information for CORNERSTONE ® PSR CERVICAL FUSION SYSTEM-SISTEMA DE FUSION CERVICAL CORNESTONE® (CORNERSTONE ® PSR CERVICAL FUSION SYSTEM-SISTEMA DE FUSION CERVICAL CORNESTONE®) in the Colombia medical device market through Pure Global AI's free database. This IIb medical device is registered under INVIMA analysis ID d5b108dcec6eafbfa9715f6bd8069f7f and manufactured by MEDTRONIC INC. The device was registered on October 26, 2033.

This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

Free Database
Powered by Pure Global AI
INVIMA Official Data
IIb
d5b108dcec6eafbfa9715f6bd8069f7f
CORNERSTONE ® PSR CERVICAL FUSION SYSTEM-SISTEMA DE FUSION CERVICAL CORNESTONE®
INVIMA Analysis ID: d5b108dcec6eafbfa9715f6bd8069f7f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

LOS DISPOSITIVOS CORNERSTONE-SR® SON JAULAS PEEK (POLIÉTER-ÉTER-CETONA) DE LONGITUDES, ANCHURAS Y FORMAS DIFERENTES, LAS CUALES SE INSERTAN ENTRE DOS CUERPOS VERTEBRALES DEL RAQUIS CERVICAL, PARA PROPORCIONAR EL SOPORTE Y LA CORRECCIÓN DURANTE LAS INTERVENCIONES QUIRÚRGICAS DE FUSIÓN ENTRE LOS CUERPOS VERTEBRALES. LA FORMA HUECA QUE TIENEN ESTOS IMPLANTES PERMITE EL RELLENO IN SITU. PARA EL RELLENO UTILIZAR UN INJERTO ÓSEO AUTÓGENO O UN MATERIAL DE SUBSTITUCIÓN ÓSEA

English

CORNERSTONE-SR® DEVICES ARE PEEK (POLYETHER-ETHER-KETONE) CAGES OF DIFFERENT LENGTHS, WIDTHS AND SHAPES, WHICH ARE INSERTED BETWEEN TWO VERTEBRAL BODIES OF THE CERVICAL SPINE, TO PROVIDE SUPPORT AND CORRECTION DURING SURGICAL PROCEDURES TO FUSE BETWEEN THE VERTEBRAL BODIES. THE HOLLOW SHAPE OF THESE IMPLANTS ALLOWS FOR IN-SITU FILLING. FOR THE FILLING, USE AN AUTOLOGOUS BONE GRAFT OR BONE REPLACEMENT MATERIAL

Device Classification
Risk Class / Clase de Riesgo
IIb
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
d5b108dcec6eafbfa9715f6bd8069f7f
Expire Date
October 26, 2033
Authorized Company / Fabricante
Name (Spanish)
MEDTRONIC INC
Name (English)
MEDTRONIC INC