K240262
- 510(k) number
- K240262
- Device name
- BTI Interna 3.0 Dental Implant System UnicCa®
- Applicant
- B.T.I. Biotechnology Institute, Sl. ES
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-10-10
- Date received
- 2024-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240262.pdf
Official FDA record: K240262
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.