FDA 510(k) Applications Submitted by NACH DAVE

FDA 510(k) Number Submission Date Device Name Applicant
K131481 05/22/2013 FREEDOM PCK COMPONENTS MAXX ORTHOPEDICS, INC.
K111785 06/24/2011 FREEDOM(R) STEMMED TIBIAL COMPONENTS MAXX ORTHOPEDICS, INC.


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