K262075
- 510(k) number
- K262075
- Device name
- Lapidus Screw Kit
- Applicant
- Relja Innovations, LLC WI · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2026-07-22
- Date received
- 2026-06-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K262075.pdf
Official FDA record: K262075
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.