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 |