The following data is part of a premarket notification filed by In2bones Sas with the FDA for Neoview Plating System.
Device ID | K160995 |
510k Number | K160995 |
Device Name: | NEOVIEW Plating System |
Classification | Plate, Fixation, Bone |
Applicant | In2Bones SAS 28 Chemin Du Petit Bois Ecully, FR 69130 |
Contact | Morgane Grenier |
Correspondent | Norman F Estrin Estrin Consulting Group LLC 9109 Copenhaver Drive Potomac, MD 20854 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-08 |
Decision Date | 2016-06-10 |
Summary: | summary |