meddevicedb.com FDA Device Reference

U2 Total Knee System- Additional Sizes

K150829 Class II Traditional
Decision Date
2015-09-25
Sponsor / Applicant
United Orthopedic Corporation

Technical Specification

510(k) Submission ID K150829
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2015-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

U2 Total Knee System- Additional Sizes received FDA 510(k) clearance under submission number K150829, sponsored by United Orthopedic Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.