meddevicedb.com FDA Device Reference

PROTRACT PRESS FIT HIP STEM

K003447 Class II Traditional
Decision Date
2000-12-15
Sponsor / Applicant
Stelkast Company

Technical Specification

510(k) Submission ID K003447
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2000-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTRACT PRESS FIT HIP STEM received FDA 510(k) clearance under submission number K003447, sponsored by Stelkast Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-12-15.

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.