K240754 is an FDA 510(k) clearance for the N2. This device is classified as a Unit, Operative Dental (Class I - General Controls, product code EIA).
Submitted by Megagen Implant Co., Ltd. (Daegu, KR). The FDA issued a Cleared decision on March 21, 2024, 1 day after receiving the submission on March 20, 2024.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6640.
| 510(k) Number | K240754 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 20, 2024 |
| Decision Date | March 21, 2024 |
| Days to Decision | 1 days |
| Submission Type | Special |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EIA — Unit, Operative Dental |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.6640 |