The following data is part of a premarket notification filed by Gm Dos Reis Industria E Comerico Ltda. with the FDA for Mini And Micro Fragments Reconstruction System – Gmreis.
| Device ID | K182718 |
| 510k Number | K182718 |
| Device Name: | Mini And Micro Fragments Reconstruction System – GMReis |
| Classification | Plate, Fixation, Bone |
| Applicant | Gm Dos Reis Industria E Comerico Ltda. Avenida Pierre Simon De La Place 600 Campinas, BR 13069320 |
| Contact | Paula Oliveira |
| Correspondent | Paula Oliveira Passarini Regulatory Affairs Of America, LLC 201 S. Biscayne Blvd. Suite 1200 Miami, FL 33131 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-09-28 |
| Decision Date | 2019-12-23 |
| Summary: | summary |