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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name screw, fixation, bone
510(k) Number K051309
Device Name ROI FUSION RODS & PLATES
Applicant
REILEY ORTHOPAEDICS, INC.
1001 OAKWOOD BLVD.
ROUND ROCK,  TX  78681
Applicant Contact J.D. WEBB
Correspondent
REILEY ORTHOPAEDICS, INC.
1001 OAKWOOD BLVD.
ROUND ROCK,  TX  78681
Correspondent Contact J.D. WEBB
Regulation Number888.3040
Classification Product Code
HWC  
Date Received05/19/2005
Decision Date 07/11/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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