FDA 510(k) Applications Submitted by Miami Device Solutions, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K161058 04/15/2016 Cannulated Screw MIAMI DEVICE SOLUTIONS, LLC
K161292 05/09/2016 Distal Radius Plating System MIAMI DEVICE SOLUTIONS, LLC
K172786 09/15/2017 MDS Plating System Miami Device Solutions, LLC
K162635 09/21/2016 Distal Radius Plating System Miami Device Solutions, LLC
K182810 10/03/2018 Distal Radius Plating System Miami Device Solutions, LLC
K162898 10/17/2016 Olecranon Plating System MIAMI DEVICE SOLUTIONS, LLC


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