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ADVANCED HIP ASSESSMENT SOFTWARE

K011917 Class II Traditional
Decision Date
2001-08-03
Sponsor / Applicant
Ge Lunar Corp.

Technical Specification

510(k) Submission ID K011917
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 2001-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCED HIP ASSESSMENT SOFTWARE received FDA 510(k) clearance under submission number K011917, sponsored by Ge Lunar Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-08-03.

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.