The following data is part of a premarket notification filed by Imagine Milling Technologies, Llc with the FDA for Mist Ic.
Device ID | K222368 |
510k Number | K222368 |
Device Name: | MIST IC |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | Imagine Milling Technologies, LLC 14220 Sullyfield Circle, Suite B Chantilly, VA 20151 |
Contact | Felix Chung |
Correspondent | Kevin A Thomas PaxMed International, LLC 12264 EL Camino Real, Suite 400 San Diego, CA 92130 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-08-05 |
Decision Date | 2022-12-01 |