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FDA 510(k) Applications Submitted by LEON BROWN II
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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