K232750
- 510(k) number
- K232750
- Device name
- BTI Interna Prosthetic Components
- Applicant
- B.T.I. Biotechnology Institute, Sl. ES
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2023-12-08
- Date received
- 2023-09-08
- 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: K232750.pdf
Official FDA record: K232750
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.