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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
510(k) Number K083772
Device Name COLUMBUS REVISION KNEE SYSTEM
Applicant
AESCULAP IMPLANT SYSTEM, INC.
3773 Corporate Parkway
Center Valley,  PA  18034
Applicant Contact LISA M BOYLE
Correspondent
AESCULAP IMPLANT SYSTEM, INC.
3773 Corporate Parkway
Center Valley,  PA  18034
Correspondent Contact LISA M BOYLE
Regulation Number888.3560
Classification Product Code
JWH  
Date Received12/18/2008
Decision Date 06/04/2009
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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