meddevicedb.com FDA Device Reference

Conformity Stem Extension Line

K242249 Class II Special
Decision Date
2024-08-30
Sponsor / Applicant
United Orthopedic Corporation

Technical Specification

510(k) Submission ID K242249
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 2024-08-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Conformity Stem Extension Line received FDA 510(k) clearance under submission number K242249, sponsored by United Orthopedic Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-08-30.

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.