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Klassic HD® Hip System

K171962 Class II Special
Decision Date
2017-07-24
Sponsor / Applicant
Total Joint Othopedics, Inc.

Technical Specification

510(k) Submission ID K171962
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2017-07-24
Clearance Pathway Special

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 K171962, sponsored by Total Joint Othopedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-07-24.

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.