FDA 510(k) Application Details - K092564

Device Classification Name	More FDA Info for this Device
510(K) Number	K092564
Device Name	O-ARM IMAGING SYSTEM
Applicant	MEDTRONIC NAVIGATION, INC. (LITTLETON) 300 FOSTER STREET LITTLETON, MA 01460 US Other 510(k) Applications for this Company
Contact	SETH KUZDZAL Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OXO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/20/2009
Decision Date	06/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review