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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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