meddevicedb.com FDA Device Reference

PARADIGM FEMORAL STEM, PERFECTA TOTAL HIP SYSTEM

K931423 Class II Traditional
Decision Date
1994-10-13
Sponsor / Applicant
Orthomed

Technical Specification

510(k) Submission ID K931423
Product Code LWJ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1994-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARADIGM FEMORAL STEM, PERFECTA TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K931423, sponsored by Orthomed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-10-13.

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.