The following data is part of a premarket notification filed by Mci Medical Concept Innovation Inc. with the FDA for Mci - Cmf System.
Device ID | K182758 |
510k Number | K182758 |
Device Name: | MCI - CMF System |
Classification | Plate, Bone |
Applicant | MCI Medical Concept Innovation Inc. 4592 North Hiatus Road Sunrise, FL 33351 |
Contact | Carlos Lacerda |
Correspondent | Janine Treter Passarini Regulatory Affairs Of America LLC 201 Biscayne Blvd, Suite 1200 Miami, FL 33131 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-28 |
Decision Date | 2019-12-05 |