meddevicedb.com FDA Device Reference

M.U.S.T. Pedicle Screw Extension and Long Tab Implants

K203482 Class II Traditional
Decision Date
2021-01-26
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K203482
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2021-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

M.U.S.T. Pedicle Screw Extension and Long Tab Implants received FDA 510(k) clearance under submission number K203482, 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 2021-01-26.

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.