FDA 510(k) Applications Submitted by MARKKU BIEDERMANN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161058 | 04/15/2016 | Cannulated Screw | MIAMI DEVICE SOLUTIONS, LLC |
| K161292 | 05/09/2016 | Distal Radius Plating System | MIAMI DEVICE SOLUTIONS, LLC |
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