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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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