meddevicedb.com FDA Device Reference

Neo Total Knee System

K142388 Class II Traditional
Decision Date
2014-12-05
Sponsor / Applicant
New Era Orthopedics, LLC

Technical Specification

510(k) Submission ID K142388
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2014-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Neo Total Knee System received FDA 510(k) clearance under submission number K142388, sponsored by New Era Orthopedics, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-12-05.

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.