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DEPUY TRI-LOCK HIP STEM

K974740 Class II Traditional
Decision Date
1998-03-18
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K974740
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1998-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEPUY TRI-LOCK HIP STEM received FDA 510(k) clearance under submission number K974740, sponsored by Depuy, 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 1998-03-18.

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.