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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Appliance, Fixation, Spinal Intervertebral Body
510(k) Number K150036
Device Name Blue Mountain Cervical Plate System
Applicant
Spineway
7 Allee Moulin Berger
Ecully,  FR 69130
Applicant Contact JULIEN THAO MY
Correspondent
Rich Jansen, Pharm.D.
11821 Bramble Cove Dr.
Fr. Myers,  FL  33905
Correspondent Contact RICH JANSEN
Regulation Number888.3060
Classification Product Code
KWQ  
Date Received01/09/2015
Decision Date 05/07/2015
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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