FDA 510(k) Applications Submitted by LEON BROWN II, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
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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