SISTEMA ESPINAL CLYDEDALE PTC
EL SISTEMA VERTEBRAL CLYDESDALE PTC™ ESTÁ FORMADO POR ARMAZONES DE PEEK REVESTIDOS DE TITANIO PURO COMERCIALMENTE (CP TI) DE DIFERENTES ANCHURAS Y ALTURAS, QUE INCLUYEN MARCADORES DE TANTALIO. ESTOS DISPOSITIVOS PUEDEN INTRODUCIRSE ENTRE DOS CUERPOS VERTE
THE CLYDESDALE PTC™ VERTEBRAL SYSTEM IS MADE UP OF COMMERCIALLY PURE TITANIUM (CP TI) COATED PEEK FRAMES OF VARYING WIDTHS AND HEIGHTS, INCLUDING TANTALUM MARKERS. THESE DEVICES CAN BE INSERTED BETWEEN TWO BODIES VERTE
- 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 DE FUSIÓN INTERSOMÁTICA
- Trade Name (English)
- INTERBODY FUSION SYSTEM
- Analysis ID
- 1402C2019 SSA
- Registration Date
- July 19, 2019
- Name (Spanish)
- MEDTRONIC, S. DE R.L. DE C.V.
- Name (English)
- MEDTRONIC, S. DE R.L. DE C.V.
Access comprehensive regulatory information for SISTEMA ESPINAL CLYDEDALE PTC (ESPINAL CLYDEDALE PTC 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 1402C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on July 19, 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.