SISTEMA DE VÁSTAGO CEMENTADO Y NO CEMENTADO POLARSTEM
LOS VÁSTAGOS FEMORALES POLARSTEM ESTÁNDAR, LATERALES Y EN VALGO ESTÁN INDICADOS PARA: - DEGENERACIÓN AVANZADA DE LA ARTICULACIÓN DE LA CADERA A CONSECUENCIA DE ARTRITIS DEGENERATIVA, POSTRAUMÁTICA O REUMATOIDE. - FRACTURA O NECROSIS AVASCULAR DE LA CABE
POLARSTEM STANDARD, LATERAL AND VALGUS FEMORAL STEMS ARE INDICATED FOR: - ADVANCED DEGENERATION OF THE HIP JOINT AS A RESULT OF DEGENERATIVE, POST-TRAUMATIC OR RHEUMATOID ARTHRITIS. - FRACTURE OR AVASCULAR NECROSIS OF THE CABE
- 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)
- PRÓTESIS DE CADERA
- Trade Name (English)
- HIP PROSTHESIS
- Analysis ID
- 793C2018 SSA
- Registration Date
- March 21, 2018
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for SISTEMA DE VÁSTAGO CEMENTADO Y NO CEMENTADO POLARSTEM (POLARSTEM CEMENTED AND NON-CEMENTED STEM 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 793C2018 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on March 21, 2018.
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.