ANVISA registration 80263050030Valid until Oct 17, 2026Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
ANVISA Registration Number: 80263050030GLOBUS MEDICAL BRASIL LTDAALPHATEC SPINE INCRisk Class III
Device names
- Technical name
- Posterior spinal system for fixation in lamina, pedicle, apophysis or articular mass.
- Risk class
- Class III
PT: Sistema posterior de coluna para fixação em lâmina, pedículo, apófise ou maciço articular.
Registration details
- Registration Number
- 80263050030
- Process Number
- 25351009189201697
- CNPJ
- 07131437000103
Company information
- Registration Holder
- GLOBUS MEDICAL BRASIL LTDA
- Manufacturer
- ALPHATEC SPINE INC
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Oct 17, 2016
- Validity
- 17/10/2026
- Last Updated
- 08/18/2026 19:00:00
About this record
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 80263050030 and manufactured by ALPHATEC SPINE INC. The registration is held by GLOBUS MEDICAL BRASIL LTDA with validity until Oct 17, 2026.
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