FDA 510(k) Applications Submitted by Bonebridge AG

FDA 510(k) Number Submission Date Device Name Applicant
K203002 10/01/2020 SALGINA 2.5mm Volar Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, TAMlNA 3.5mm Proximal Humerus System, TRIFT 3.5mm 1/3 Tubular System Bonebridge AG
K213864 12/10/2021 Bonebridge Osteosynthesis Plating System Bonebridge AG
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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