K240202
- 510(k) number
- K240202
- Device name
- Conical Platform Dental Implants System
- Applicant
- Noris Medical , Ltd. IL
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-06-06
- Date received
- 2024-01-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240202.pdf
Official FDA record: K240202
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.