K231803
- 510(k) number
- K231803
- Device name
- Neodent Implant System - Zirconia Implant System
- Applicant
- JJGC Indústria e Comércio de Materiais Dentários S.A. BR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2023-12-13
- Date received
- 2023-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231803.pdf
Official FDA record: K231803
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.