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SPY INTRA-OPERATIVE IMAGING SYSTEM, MODEL SP2000

K071037 Class II Special
Decision Date
2007-05-10
Sponsor / Applicant
Novadaq Technologies, Inc.

Technical Specification

510(k) Submission ID K071037
Product Code IZI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1600
Decision Date 2007-05-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPY INTRA-OPERATIVE IMAGING SYSTEM, MODEL SP2000 received FDA 510(k) clearance under submission number K071037, sponsored by Novadaq Technologies, 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 2007-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code IZI and 21 CFR 892.1600, within the Radiology review panel as a Class II device.