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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name orthosis, spinal pedicle fixation
510(K) Number K122233
Device Name CAPSURE(R) PS SYSTEM
Applicant
SPINE WAVE, INC.
three enterprise dr.
suite 210
shelton,  CT  06484
Contact joseph mercado
Regulation Number888.3070
Classification Product Code
MNI  
Subsequent Product Code
MNH  
Date Received07/26/2012
Decision Date 10/11/2012
Decision substantially equivalent (SE)
Classification Advisory Committee Orthopedic
Review Advisory Committee Orthopedic
summary summary
Type Special
Reviewed by Third Party No
Expedited Review No
Combination Product No
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