The following data is part of a premarket notification filed by Gm Dos Reis Industria E Comerico Ltda with the FDA for Pedimax Ii - Pedicular Screw Spinal System.
| Device ID | K180626 |
| 510k Number | K180626 |
| Device Name: | Pedimax II - Pedicular Screw Spinal System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Gm Dos Reis Industria E Comerico Ltda Avenida Pierre Simon De LaPlace, 600 Campinas, BR 13069320 |
| Contact | Paula Oliveira |
| Correspondent | Mauro Malzyner Passarini Regulatory Affairs Of America, LLC 201 S. Biscayne Blvd. Suite 1200 Miami, FL 33131 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-03-09 |
| Decision Date | 2019-02-01 |