meddevicedb.com FDA Device Reference

Mecta-C Stand Alone

K192906 Class II Traditional
Decision Date
2020-03-04
Sponsor / Applicant
Medacta International S.A.

Technical Specification

510(k) Submission ID K192906
Product Code OVE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2020-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Mecta-C Stand Alone received FDA 510(k) clearance under submission number K192906, 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 2020-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code OVE and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.