K223113
- 510(k) number
- K223113
- Device name
- Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments
- Applicant
- Medentika GmbH DE
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-04-15
- Date received
- 2022-10-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K223113.pdf
Official FDA record: K223113
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.