The following data is part of a premarket notification filed by Jjgc Industria E Comercio De Materiais Dentarios Sa with the FDA for Neodent Implant System - Gm Line.
Device ID | K163194 |
510k Number | K163194 |
Device Name: | Neodent Implant System - GM Line |
Classification | Implant, Endosseous, Root-form |
Applicant | JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS SA AV. JUSCELINO KUBITSCHEK DE OLIVEIRA, 3291 - CIC Curitiba, BR 81270-200 |
Contact | Julianne Lechechem |
Correspondent | Jennifer M. Jackson STRAUMANN USA, INC. 60 MINUTEMAN ROAD Andover, MA 01810 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-11-15 |
Decision Date | 2017-07-14 |
Summary: | summary |