meddevicedb.com FDA Device Reference

FMP Extended Liners

K172651 Class II Traditional
Decision Date
2017-12-13
Sponsor / Applicant
Encore Medical L.P.

Technical Specification

510(k) Submission ID K172651
Product Code OQG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2017-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FMP Extended Liners received FDA 510(k) clearance under submission number K172651, sponsored by Encore Medical L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-12-13.

Classification & Regulation

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