K192062 is an FDA 510(k) clearance for the Nucleoss T6 Dental Implant System. This device is classified as a Implant, Endosseous, Root-form (Class II - Special Controls, product code DZE).
Submitted by Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST (Izmir, TR). The FDA issued a Cleared decision on August 27, 2020, 392 days after receiving the submission on August 1, 2019.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3640.
| 510(k) Number | K192062 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 01, 2019 |
| Decision Date | August 27, 2020 |
| Days to Decision | 392 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 |