FDA 510(k) Applications Submitted by Michelle Gumpelmayer
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231292 | 05/04/2023 | TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE 3.5mm Distal Humerus System | Bonebridge AG |
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