K234049
- 510(k) number
- K234049
- Device name
- Straumann® BLC and TLC Implants - Line extension
- Applicant
- Institut Straumann AG CH
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-03-20
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K234049.pdf
Official FDA record: K234049
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.