meddevicedb.com FDA Device Reference

U1 HIP SYSTEM - BIPOLAR

K050269 Class II Traditional
Decision Date
2005-08-29
Sponsor / Applicant
United Orthopedic Corp.

Technical Specification

510(k) Submission ID K050269
Product Code KWY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3390
Decision Date 2005-08-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

U1 HIP SYSTEM - BIPOLAR received FDA 510(k) clearance under submission number K050269, 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 2005-08-29.

Classification & Regulation

This clearance is catalogued under FDA product code KWY and 21 CFR 888.3390, within the Orthopedic review panel as a Class II device.