K242432 is an FDA 510(k) clearance for the MT-Bone. This device is classified as a Drill, Bone, Powered (Class II - Special Controls, product code DZI).
Submitted by Mectron S.P.A. (Carasco, IT). The FDA issued a Cleared decision on August 19, 2024, 3 days after receiving the submission on August 16, 2024.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4120.
| 510(k) Number | K242432 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 16, 2024 |
| Decision Date | August 19, 2024 |
| Days to Decision | 3 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | DZI - Drill, Bone, Powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.4120 |