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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Intervertebral Fusion Device With Integrated Fixation, Cervical
510(k) Number K150913
Device Name INCITE ANCHORED CERVICAL INTERBODY DEVICE
Applicant
Incite Innovation
1500 Main St., Suite 2410
Springfield,  MA  01115 -5707
Applicant Contact JOHN KIRWAN
Correspondent
Alphatec Spine, Inc.
5818 El Camino Real
Carlsnad,  CA  92008
Correspondent Contact RENEE MURPHY
Regulation Number888.3080
Classification Product Code
OVE  
Date Received04/06/2015
Decision Date 04/30/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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