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PROCLASS PRESS FIT HIP STEM

K032110 Class II Traditional
Decision Date
2003-09-22
Sponsor / Applicant
Stelkast Company

Technical Specification

510(k) Submission ID K032110
Product Code LWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 2003-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCLASS PRESS FIT HIP STEM received FDA 510(k) clearance under submission number K032110, 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 2003-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code LWJ and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.