K230104
- 510(k) number
- K230104
- Device name
- Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
- Applicant
- Anthogyr FR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2023-10-16
- Date received
- 2023-01-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K230104.pdf
Official FDA record: K230104
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.