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Klassic HD Hip System

K151440 Class II Traditional
Decision Date
2015-09-03
Sponsor / Applicant
Total Joint Orthopedics, Inc.

Technical Specification

510(k) Submission ID K151440
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2015-09-03
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 K151440, sponsored by Total Joint 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 2015-09-03.

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.