K242861
- 510(k) number
- K242861
- Device name
- TrueLok Elevate
- Applicant
- Orthofix Srl IT
- Product code
- KTT — Appliance, Fixation, Nail/Blade/Plate Combination, M
- Decision date
- 2024-12-03
- Date received
- 2024-09-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K242861.pdf
Official FDA record: K242861
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.