K231127 is an FDA 510(k) clearance for the S.I.N. Dental Implant System. This device is classified as a Implant, Endosseous, Root-form (Class II - Special Controls, product code DZE).
Submitted by S.I.N. ? Sistema DE Implante Nacional S.A. (São Paulo, BR). The FDA issued a Cleared decision on December 7, 2023, 231 days after receiving the submission on April 20, 2023.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3640.
| 510(k) Number | K231127 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 20, 2023 |
| Decision Date | December 07, 2023 |
| Days to Decision | 231 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | DZE - Implant, Endosseous, Root-form |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3640 |