The following data is part of a premarket notification filed by Materialise Dental Nv with the FDA for Simplant Navigator Personalized Dental Care System.
Device ID | K112679 |
510k Number | K112679 |
Device Name: | SIMPLANT NAVIGATOR PERSONALIZED DENTAL CARE SYSTEM |
Classification | System, Image Processing, Radiological |
Applicant | MATERIALISE DENTAL NV TECHNOLOGIELAAN 15 Leuven, BE 3001 |
Contact | Carl Van Lierde |
Correspondent | Carl Van Lierde MATERIALISE DENTAL NV TECHNOLOGIELAAN 15 Leuven, BE 3001 |
Product Code | LLZ |
Subsequent Product Code | DZA |
Subsequent Product Code | NDP |
Subsequent Product Code | NOF |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-09-14 |
Decision Date | 2012-02-22 |
Summary: | summary |