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DXAVIEW SPINE AND HIP, MODEL QCT-3D PLUS

K031991 Class II Special
Decision Date
2003-07-30
Sponsor / Applicant
Image Analysis, Inc.

Technical Specification

510(k) Submission ID K031991
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 2003-07-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DXAVIEW SPINE AND HIP, MODEL QCT-3D PLUS received FDA 510(k) clearance under submission number K031991, sponsored by Image Analysis, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code KGI and 21 CFR 892.1170, within the Radiology review panel as a Class II device.