meddevicedb.com FDA Device Reference

LINEAGE A-CLASS POLY LINER

K052026 Class II Traditional
Decision Date
2005-12-05
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K052026
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2005-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LINEAGE A-CLASS POLY LINER received FDA 510(k) clearance under submission number K052026, 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 2005-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.