meddevicedb.com FDA Device Reference

VECTRIX EXTERNAL FIXATOR

K140649 Class II Abbreviated
Decision Date
2014-12-29
Sponsor / Applicant
3D Medical Concepts, LLC

Technical Specification

510(k) Submission ID K140649
Product Code NDK
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2014-12-29
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VECTRIX EXTERNAL FIXATOR received FDA 510(k) clearance under submission number K140649, sponsored by 3D Medical Concepts, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code NDK and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.