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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceREFLECTION CERAMIC ACETABULAR SYSTEM
Generic NameProsthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
ApplicantSmith & Nephew, Inc.
1450 Brooks Road
Memphis, TN 38116
PMA NumberP030022
Supplement NumberS002
Date Received02/14/2006
Decision Date06/16/2006
Withdrawal Date 08/31/2022
Product Code MRA 
Advisory Committee Orthopedic
Supplement Type135 Review Track For 30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR MANUFACTURING PROCESS CHANGES TO BE MADE BY CERAMTEC, INC., FOR THE BIOLOX FORTE CERAMIC FEMORAL HEADS AND INSERTS.
Post-Approval StudyShow Report Schedule and Study Progress
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