The following data is part of a premarket notification filed by Ortho Organizers, Inc. with the FDA for Ceramic Brackets.
Device ID | K110335 |
510k Number | K110335 |
Device Name: | CERAMIC BRACKETS |
Classification | Bracket, Ceramic, Orthodontic |
Applicant | ORTHO ORGANIZERS, INC. 1822 ASTON AVENUE Carlsbad, CA 92008 -7603 |
Contact | Foster Boop |
Correspondent | Foster Boop ORTHO ORGANIZERS, INC. 1822 ASTON AVENUE Carlsbad, CA 92008 -7603 |
Product Code | NJM |
CFR Regulation Number | 872.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-02-04 |
Decision Date | 2011-05-19 |
Summary: | summary |