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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
510(k) Number K131030
Device Name RANGE SPINAL SYSTEM
Applicant
K2m,Inc.
751 Miller Dr., SE, Suite F1
Leesburg,  VA  20175
Applicant Contact NANCY GIEZEN
Correspondent
K2m,Inc.
751 Miller Dr., SE, Suite F1
Leesburg,  VA  20175
Correspondent Contact NANCY GIEZEN
Regulation Number888.3070
Classification Product Code
OSH  
Subsequent Product Codes
KWP   MNH   MNI  
Date Received04/12/2013
Decision Date 05/09/2013
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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