K262253
- 510(k) number
- K262253
- Device name
- Lantern Knee Navigation Unit (406000-03);Lantern Hip Navigation Unit (502000-03)
- Applicant
- Orthalign, Inc. CA · US
- Product code
- ONN — Intraoperative Orthopedic Joint Assessment Aid
- Decision date
- 2026-07-31
- Date received
- 2026-07-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K262253.pdf
Official FDA record: K262253
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.