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Klassic HD Hip System

K161073 Class II Traditional
Decision Date
2016-10-19
Sponsor / Applicant
Total Joint Othopedics, Inc.

Technical Specification

510(k) Submission ID K161073
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2016-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Klassic HD Hip System received FDA 510(k) clearance under submission number K161073, sponsored by Total Joint Othopedics, 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 2016-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.