meddevicedb.com FDA Device Reference

UCP Stem

K152530 Class II Traditional
Decision Date
2016-03-14
Sponsor / Applicant
United Orthopedic Corporation

Technical Specification

510(k) Submission ID K152530
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2016-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UCP Stem received FDA 510(k) clearance under submission number K152530, sponsored by United Orthopedic Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-03-14.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.