meddevicedb.com FDA Device Reference

ORTHOHUB EXTERNAL FIXATOR SOFTWARE

K140550 Class II Traditional
Decision Date
2014-08-25
Sponsor / Applicant
Orthohub, Inc.

Technical Specification

510(k) Submission ID K140550
Product Code OSN
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2014-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOHUB EXTERNAL FIXATOR SOFTWARE received FDA 510(k) clearance under submission number K140550, sponsored by Orthohub, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-08-25.

Classification & Regulation

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