meddevicedb.com FDA Device Reference

Meta+ Bone Cement & M.U.S.T. Fenestrated Pedicle Screw System

K241034 Class II Traditional
Decision Date
2024-06-12
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K241034
Product Code PML
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3027
Decision Date 2024-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Meta+ Bone Cement & M.U.S.T. Fenestrated Pedicle Screw System received FDA 510(k) clearance under submission number K241034, 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 2024-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code PML and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.