Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. - ANVISA Registration 80502380001

Access comprehensive regulatory information for Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass. in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80502380001 and manufactured by AMEDICA CORPORATION. The registration is held by SINTEX MEDICAL IMPLANT BIOMEDICA COMERCIAL LTDA with validity until Jul 24, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ORTHOFIX INC., NEOORTHO PRODUTOS ORTOPÉDICOS S/A, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.