K233721
- 510(k) number
- K233721
- Device name
- KLS Martin Drill-Free MMF Screw
- Applicant
- KLS-Martin L.P. FL · US
- Product code
- DZL — Screw, Fixation, Intraosseous
- Decision date
- 2024-09-17
- Date received
- 2023-11-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233721.pdf
Official FDA record: K233721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.