The following data is part of a premarket notification filed by Tp Orthodontics, Inc. with the FDA for Ceramaflex Bracket System.
Device ID | K950992 |
510k Number | K950992 |
Device Name: | CERAMAFLEX BRACKET SYSTEM |
Classification | Bracket, Ceramic, Orthodontic |
Applicant | TP ORTHODONTICS, INC. 100 CENTER PLAZA Laporte, IN 46350 -0073 |
Contact | Nancy S Iatarola |
Correspondent | Nancy S Iatarola TP ORTHODONTICS, INC. 100 CENTER PLAZA Laporte, IN 46350 -0073 |
Product Code | NJM |
CFR Regulation Number | 872.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-03 |
Decision Date | 1995-05-03 |