FDA 510(k) Application Details - K082795

Device Classification Name	System, Facet Screw Spinal Device   More FDA Info for this Device
510(K) Number	K082795
Device Name	System, Facet Screw Spinal Device
Applicant	INTERVENTIONAL SPINE, INC. 13700 ALTON PKWY., SUITE 160 IRVINE, CA 92618 US Other 510(k) Applications for this Company
Contact	CAROL EMERSON Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MRW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/23/2008
Decision Date	12/12/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review