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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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