Firebird® Spinal Fixation Systems: Firebird System +6 more— 510(k) K180179

Substantially Equivalent

Orthofix, Inc.

FDA 510(k) clearance K180179 for Firebird® Spinal Fixation Systems: Firebird System +6 more, Substantially Equivalent on 2018-08-24. Applicant: Orthofix, Inc.. Device class: 2.

Clearance details

Device name as filed
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
Applicant
Orthofix, Inc.
Product code
Code NKB
Device class
Class 2
Regulation
21 CFR 888.3070
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lewisville, TX, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code NKB

product code NKB
Death
27
Injury
5,033
Malfunction
4,140
Total
9,200

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.