K242616
- 510(k) number
- K242616
- Device name
- Lantern® Hip
- Applicant
- Orthalign, Inc. CA · US
- Product code
- ONN — Intraoperative Orthopedic Joint Assessment Aid
- Decision date
- 2024-10-03
- Date received
- 2024-09-03
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K242616.pdf
Official FDA record: K242616
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.