meddevicedb.com FDA Device Reference

Tahoe Uni Knee System

K170344 Class II Traditional
Decision Date
2017-10-05
Sponsor / Applicant
Consensus Orthopedics, Inc.

Technical Specification

510(k) Submission ID K170344
Product Code HSX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3520
Decision Date 2017-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tahoe Uni Knee System received FDA 510(k) clearance under submission number K170344, sponsored by Consensus Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code HSX and 21 CFR 888.3520, within the Orthopedic review panel as a Class II device.