K260112
- 510(k) number
- K260112
- Device name
- QuikFix External Fixator: Knee-Spanning Pack
- Applicant
- Stabiliz Orthopaedics, Inc. PA · US
- Product code
- KTT — Appliance, Fixation, Nail/Blade/Plate Combination, M
- Decision date
- 2026-03-23
- Date received
- 2026-01-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260112.pdf
Official FDA record: K260112
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.