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 |