FDA 510(k) Applications Submitted by BIOMET, INC

FDA 510(k) Number Submission Date Device Name Applicant
K161190 04/27/2016 G7 Dual Mobility System, Active Articulation System Biomet, Inc
K171054 04/10/2017 Biomet Knee Joint Replacement Prostheses Biomet, Inc
K183553 12/20/2018 Compress and Mini Compress Anti-Rotation Spindles Biomet, Inc


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact