FDA 510(k) Applications Submitted by Biomet Manufacturing Corp

FDA 510(k) Number Submission Date Device Name Applicant
K181611 06/19/2018 Comprehensive Reverse Shoulder System Biomet Manufacturing Corp
K182516 09/13/2018 Comprehensive Nano Stemless Shoulder Biomet Manufacturing Corp
K172502 08/18/2017 Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini Baseplate Biomet Manufacturing Corp


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