K253940
- 510(k) number
- K253940
- Device name
- M.U.S.T. Pedicle Screw System - Extension
- Applicant
- Medacta International S.A. CH
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2026-04-28
- Date received
- 2025-12-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253940.pdf
Official FDA record: K253940
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.