K254202
- 510(k) number
- K254202
- Device name
- MectaLIF 3D Metal Anterior
- Applicant
- Medacta International S.A. CH
- Product code
- OVD — Intervertebral Fusion Device With Integrated Fixatio
- Decision date
- 2026-05-05
- Date received
- 2025-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K254202.pdf
Official FDA record: K254202
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.