meddevicedb.com FDA Device Reference

M.U.S.T. Midline Cortical (MC) Screw System

K210427 Class II Traditional
Decision Date
2021-04-20
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K210427
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2021-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

M.U.S.T. Midline Cortical (MC) Screw System received FDA 510(k) clearance under submission number K210427, sponsored by Medacta International S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.