K231072
- 510(k) number
- K231072
- Device name
- Anthogyr FlexiBase® titanium bases for Axiom® BL
- Applicant
- Anthogyr FR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-01-04
- Date received
- 2023-04-14
- 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: K231072.pdf
Official FDA record: K231072
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.