STRYKER TRITANIUM.
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·STRYKER MÉXICO, S.A. DE C.V.·Registered August 10, 2018LA CAJA LUMBAR POSTERIOR (LP) TRITANIUM ES UN DISPOSITIVO DE FUSIÓN CORPORAL INTERVERTEBRAL INDICADO PARA EL TRATAMIENTO DE LA ESPONDILOLISTESIS, LOS TRASTORNOS DEGENERATIVOS VERTEBRALES Y LA INESTABILIDAD DISCAL Y VERTEBRAL, Y TAMBIÉN SE PUEDE UTILIZAR E
THE POSTERIOR LUMBAR CAGE (LP) TRITANIUM IS AN INTERVERTEBRAL BODY FUSION DEVICE INDICATED FOR THE TREATMENT OF SPONDYLOLISTHESIS, VERTEBRAL DEGENERATIVE DISORDERS AND DISC AND VERTEBRAL INSTABILITY, AND CAN ALSO BE USED IN
- 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)
- CAJA LUMBAR POSTERIOR.
- Trade Name (English)
- POSTERIOR LUMBAR BOX.
- Analysis ID
- 1998C2018 SSA
- Registration Date
- August 10, 2018
- Name (Spanish)
- STRYKER MÉXICO, S.A. DE C.V.
- Name (English)
- STRYKER MEXICO, S.A. DE C.V.
Access comprehensive regulatory information for STRYKER TRITANIUM. (STRYKER TRITANIUM.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1998C2018 SSA and manufactured by STRYKER MÉXICO, S.A. DE C.V.. The device was registered on August 10, 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.