meddevicedb.com FDA Device Reference

U2 ACETABULAR CUP

K022520 Class II Traditional
Decision Date
2003-02-25
Sponsor / Applicant
United Orthopedic Corp.

Technical Specification

510(k) Submission ID K022520
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2003-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

U2 ACETABULAR CUP received FDA 510(k) clearance under submission number K022520, sponsored by United Orthopedic 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 2003-02-25.

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.