The following data is part of a premarket notification filed by Dentsply Interntional with the FDA for Allure Mb Ceramic Brackets.
Device ID | K090454 |
510k Number | K090454 |
Device Name: | ALLURE MB CERAMIC BRACKETS |
Classification | Bracket, Ceramic, Orthodontic |
Applicant | DENTSPLY INTERNTIONAL 221 W. PHILADELPHIA ST. STE.60 SUSQUEHANNA COMMERCE CRT. WEST York, PA 17405 |
Contact | Helen Lewis |
Correspondent | Helen Lewis DENTSPLY INTERNTIONAL 221 W. PHILADELPHIA ST. STE.60 SUSQUEHANNA COMMERCE CRT. WEST York, PA 17405 |
Product Code | NJM |
CFR Regulation Number | 872.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-02-23 |
Decision Date | 2009-03-20 |
Summary: | summary |