meddevicedb.com FDA Device Reference

F-19 TOTAL HIP PROSTHESIS

K903234 Class II Traditional
Decision Date
1990-10-10
Sponsor / Applicant
Med-Tek Corp.

Technical Specification

510(k) Submission ID K903234
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1990-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

F-19 TOTAL HIP PROSTHESIS received FDA 510(k) clearance under submission number K903234, sponsored by Med-Tek Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.