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VANGUARD ANTERIOR STABILIZED TIBIAL BEARINGS

K050222 Class II Special
Decision Date
2005-08-16
Sponsor / Applicant
Biomet, Inc.

Technical Specification

510(k) Submission ID K050222
Product Code MBH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3565
Decision Date 2005-08-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VANGUARD ANTERIOR STABILIZED TIBIAL BEARINGS received FDA 510(k) clearance under submission number K050222, sponsored by Biomet, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code MBH and 21 CFR 888.3565, within the Orthopedic review panel as a Class II device.