meddevicedb.com FDA Device Reference

STEM HIP REPLACEMENT SYSTEM, MODEL PHA002XX

K021346 Class II Abbreviated
Decision Date
2002-07-02
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K021346
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2002-07-02
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STEM HIP REPLACEMENT SYSTEM, MODEL PHA002XX received FDA 510(k) clearance under submission number K021346, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2002-07-02.

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.