meddevicedb.com FDA Device Reference

LSF TRIAD TOTAL HIP SYSTEM

K971020 Class II Traditional
Decision Date
1997-06-18
Sponsor / Applicant
Osteoimplant Technology, Inc.

Technical Specification

510(k) Submission ID K971020
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1997-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LSF TRIAD TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K971020, sponsored by Osteoimplant Technology, 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 1997-06-18.

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.