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Interventional Spine, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K160464	Opticage(R) Expandable Interbody Fusion Device	MAX	2016-04-04	View
510(k)	K132479	OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00	MAX	2013-09-19	View
510(k)	K113527	OPTICAGE INTERBODY FUSION DEVICE	MAX	2012-01-20	View
510(k)	K090767	PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER	MRW	2009-06-11	View
510(k)	K082795	SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT	MRW	2008-12-12	View

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