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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 bone graft, cervical
510(k) Number K122588
Device Name VUSION CS PLUS
Original Applicant
ORTHO DEVELOPMENT CORP.
12187 south business park dr.
draper,  UT  84020
Original Contact tom haueter
Regulation Number888.3080
Classification Product Code
ODP  
Date Received08/24/2012
Decision Date 06/12/2013
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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