meddevicedb.com FDA Device Reference

PTA (PROGRESSIVE TIBIAL ALIGNMENT)

K060403 Class II Traditional
Decision Date
2006-03-28
Sponsor / Applicant
Meridian Medical

Technical Specification

510(k) Submission ID K060403
Product Code LXT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2006-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PTA (PROGRESSIVE TIBIAL ALIGNMENT) received FDA 510(k) clearance under submission number K060403, sponsored by Meridian Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code LXT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.