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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, Lumbar
510(k) Number K103729
Device Name INFILL INTERVERTEBRAL BODY FUSION DEVICE
Applicant
Pinnacle Spine Group, LLC
1601 Elm St.
Suite 300
Dallas,  TX  75201
Applicant Contact Rebecca K Pine
Correspondent
Pinnacle Spine Group, LLC
1601 Elm St.
Suite 300
Dallas,  TX  75201
Correspondent Contact Rebecca K Pine
Regulation Number888.3080
Classification Product Code
MAX  
Date Received12/22/2010
Decision Date 04/18/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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