The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Firebird® Spinal Fixation Systems: Firebird System; Firebird Deformity System; Firebird® Nxg Spinal Fixation System; Phoenix® Minimally Invasive Spinal Fixation System; Phoenix® Cdx™ Minimally Invasive Spinal Fixation System; Janus® Midline Fixation .
Device ID | K180179 |
510k Number | K180179 |
Device Name: | Firebird® Spinal Fixation Systems: Firebird System; Firebird Deformity System; Firebird® NXG Spinal Fixation System; Phoenix® Minimally Invasive Spinal Fixation System; Phoenix® CDX™ Minimally Invasive Spinal Fixation System; JANUS® Midline Fixation |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Contact | Jacki Koch |
Correspondent | Jacki Koch Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-01-23 |
Decision Date | 2018-08-24 |