The following data is part of a premarket notification filed by Denali Corporation with the FDA for Fusion Resin Cement And Core Kit.
Device ID | K070702 |
510k Number | K070702 |
Device Name: | FUSION RESIN CEMENT AND CORE KIT |
Classification | Material, Tooth Shade, Resin |
Applicant | DENALI CORPORATION 134 OLD WASHINGTON STREET Hanover, MA 02339 |
Contact | Jan G Stannard |
Correspondent | Jan G Stannard DENALI CORPORATION 134 OLD WASHINGTON STREET Hanover, MA 02339 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2007-03-13 |
Decision Date | 2007-05-10 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
D820ACORENOW0 | K070702 | 000 |
D820ACOREEOW0 | K070702 | 000 |