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IMMERGE IMAGE CORRELATION

K970623 Class II Traditional
Decision Date
1997-04-28
Sponsor / Applicant
Surgical Navigation Technologies, Inc.

Technical Specification

510(k) Submission ID K970623
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1997-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMERGE IMAGE CORRELATION received FDA 510(k) clearance under submission number K970623, sponsored by Surgical Navigation Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-04-28.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.