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 |
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