meddevicedb.com FDA Device Reference

MECTA-C

K112862 Class II Traditional
Decision Date
2011-12-19
Sponsor / Applicant
Medacta International

Technical Specification

510(k) Submission ID K112862
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2011-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MECTA-C received FDA 510(k) clearance under submission number K112862, sponsored by Medacta International. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-12-19.

Classification & Regulation

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