meddevicedb.com FDA Device Reference

BALANCE HIP SYSTEM

K050251 Class III Traditional
Decision Date
2005-05-27
Sponsor / Applicant
Biomet, Inc.

Technical Specification

510(k) Submission ID K050251
Product Code KWA
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3330
Decision Date 2005-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BALANCE HIP SYSTEM received FDA 510(k) clearance under submission number K050251, sponsored by Biomet, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-05-27.

Classification & Regulation

This clearance is catalogued under FDA product code KWA and 21 CFR 888.3330, within the Orthopedic review panel as a Class III device.