meddevicedb.com FDA Device Reference

TOTAL HIP PROTHESIS FEMORAL COMPONENT

K923734 Class II Traditional
Decision Date
1993-06-14
Sponsor / Applicant
Intermedics Orthopedics

Technical Specification

510(k) Submission ID K923734
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1993-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL HIP PROTHESIS FEMORAL COMPONENT received FDA 510(k) clearance under submission number K923734, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.