meddevicedb.com FDA Device Reference

ADVANCE A-CLASS TIBIAL INSERT

K081479 Class II Traditional
Decision Date
2009-02-20
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K081479
Product Code MBH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3565
Decision Date 2009-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCE A-CLASS TIBIAL INSERT received FDA 510(k) clearance under submission number K081479, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-02-20.

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.