K250764
- 510(k) number
- K250764
- Device name
- SpineLinc Anterior Cervical Implant System
- Applicant
- Lincotek Medical TN · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2025-12-05
- Date received
- 2025-03-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250764.pdf
Official FDA record: K250764
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.