FDA 510(k) Applications Submitted by MX ORTHOPEDICS, CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K161303 05/10/2016 dynaMXÖ Compression Plate MX ORTHOPEDICS, CORP.
K153129 10/30/2015 dynaMX Tabbed Staple MX Orthopedics, Corp.
K143622 12/22/2014 dynaMX Compression Staple MX Orthopedics, Corp.


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