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 |