The following data is part of a premarket notification filed by S.i.n. – Sistema De Implante Nacional S.a. with the FDA for S.i.n. Implant System.
| Device ID | K170392 |
| 510k Number | K170392 |
| Device Name: | S.I.N. Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | S.I.N. – Sistema De Implante Nacional S.A. Avenida Vereador Abel Ferreira, 1100 Sao Paulo, BR 03340-000 |
| Contact | Denis Oliveira |
| Correspondent | Linda K. Schulz PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego, CA 92130 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-02-08 |
| Decision Date | 2017-12-01 |
| Summary: | summary |