K240977
- 510(k) number
- K240977
- Device name
- DenQ Sub SLA Implant System
- Applicant
- Denq KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-09-13
- Date received
- 2024-04-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K240977.pdf
Official FDA record: K240977
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.