meddevicedb.com FDA Device Reference

FREEDOM(R) STEMMED TIBIAL COMPONENTS

K111785 Class II Traditional
Decision Date
2012-06-29
Sponsor / Applicant
Maxx Orthopedics, Inc.

Technical Specification

510(k) Submission ID K111785
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2012-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FREEDOM(R) STEMMED TIBIAL COMPONENTS received FDA 510(k) clearance under submission number K111785, sponsored by Maxx Orthopedics, 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 2012-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.