The following data is part of a premarket notification filed by Mirus, Llc with the FDA for Europa Pedicle Screw System.
Device ID | K180337 |
510k Number | K180337 |
Device Name: | EUROPA Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | MiRus, LLC 2150 Newmarket Parkway Marietta, GA 30067 |
Contact | Jordan Bauman |
Correspondent | Jordan Bauman MiRus, LLC 2150 Newmarket Parkway SE Suite 108 Marietta, GA 30067 |
Product Code | NKB |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-02-07 |
Decision Date | 2019-03-14 |