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 |