K260810
- 510(k) number
- K260810
- Device name
- Anteralign LS coverplate
- Applicant
- Tyber Medical, LLC PA · US
- Product code
- OVD — Intervertebral Fusion Device With Integrated Fixatio
- Decision date
- 2026-06-10
- Date received
- 2026-03-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K260810.pdf
Official FDA record: K260810
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.