Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Biomet Spine (Aka Ebi, LLC)

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K131615	POLARIS SPINAL SYSTEM	OSH	2013-09-04	View
510(k)	K123549	POLARIS SPINAL SYSTEM - BALLISTA II PERCUTANEOUS SCREW PLACEMENT SYSTEM	NKB	2013-02-25	View
510(k)	K123451	POLARIS SPINAL SYSTEM - BALLISTA II RODS	NKB	2012-12-03	View
510(k)	K122989	BIOMET LATERAL SPACER SYSTEM	MAX	2012-10-24	View
510(k)	K122378	NEXTGEN ALTIUS OCT SYSTEM	KWP	2012-09-20	View
510(k)	K113593	NEXTGEN ALTIUS OCT SYSTEM	KWP	2012-04-17	View
510(k)	K110650	ZYSTON ARC INTERBODY SPACER	MAX	2011-06-30	View
510(k)	K100805	GALLERY LAMINOPLASTY FIXATION SYSTEM	NQW	2010-07-20	View
510(k)	K100409	POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTUE ANTERIOR FIXATION SYSTEM	NKB	2010-06-23	View

↑