FDA 510(k) Applications Submitted by LEON BROWN

FDA 510(k) Number Submission Date Device Name Applicant
K152252 08/10/2015 Arthrex iBalance TKA System ARTHREX, INC.
K152382 08/24/2015 Arthrex iBalance TKA System ARTHREX, INC.
K153586 12/16/2015 Arthrex iBalance TKA System Arthrex, Inc.
K141635 06/19/2014 ARTHREX IBALANCE TKA SYSTEM ARTHREX, INC.
K132043 07/02/2013 ARTHREX SPEEDCINCH ARTHREX, INC.
K133854 12/19/2013 ARTHREX IBALANCE TKA SYSTEM ARTHREX, INC.


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