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. Dental Implant System.
| Device ID | K170398 | 
| 510k Number | K170398 | 
| Device Name: | S.I.N. Dental 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 03310-000 | 
| 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 | 2017-02-09 | 
| Decision Date | 2017-11-21 | 
| Summary: | summary |