FDA 510(k) Applications Submitted by Julie Largent
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160058 | 01/12/2016 | Biomet Variable Pitch Compression Screw System | Biomet Inc |
| K162424 | 08/30/2016 | Ulna Plating System | BIOMET INC |
| K133354 | 10/31/2013 | PERI-PROSTHETIC CABLE SYSTEM | BIOMET, INC. |
| K143697 | 12/24/2014 | Biomet Proximal Humerus Plating System | Biomet Manufacturing |
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