The following data is part of a premarket notification filed by Signature Orthodontics with the FDA for Signature Orthodontic System.
Device ID | K183542 |
510k Number | K183542 |
Device Name: | Signature Orthodontic System |
Classification | Bracket, Ceramic, Orthodontic |
Applicant | Signature Orthodontics 1035 Cambridge Street, Suite 14a Cambridge, MA 02141 |
Contact | Alfred Charles Griffin |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | NJM |
CFR Regulation Number | 872.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2018-12-20 |
Decision Date | 2019-01-02 |
Summary: | summary |