K260015
- 510(k) number
- K260015
- Device name
- ANTERIS Thoracolumbar Plate System
- Applicant
- SpineCraft IL · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2026-03-04
- Date received
- 2026-01-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260015.pdf
Official FDA record: K260015
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.