Last synced on 25 January 2026 at 3:41 am

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 Screw; JANUS® Fenestrated Screw

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180179
510(k) Type
Traditional
Applicant
Orthofix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2018
Days to Decision
213 days
Submission Type
Summary

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 Screw; JANUS® Fenestrated Screw

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180179
510(k) Type
Traditional
Applicant
Orthofix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2018
Days to Decision
213 days
Submission Type
Summary