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 |