FDA 510(k) Applications Submitted by BIOMET INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190035 | 01/08/2019 | Biomet Headless Compression and Twist-Off Screws | Biomet Inc |
| K172408 | 08/09/2017 | Biomet Bone Cement R | Biomet Inc |
| K160058 | 01/12/2016 | Biomet Variable Pitch Compression Screw System | Biomet Inc |
| K162424 | 08/30/2016 | Ulna Plating System | BIOMET INC |
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