K242432
- 510(k) number
- K242432
- Device name
- MT-Bone
- Applicant
- Mectron S.P.A. IT
- Product code
- DZI — Drill, Bone, Powered
- Decision date
- 2024-08-19
- Date received
- 2024-08-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K242432.pdf
Official FDA record: K242432
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.