FDA 510(k) Applications Submitted by Orthofix Medical Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K240830 03/26/2024 Reef TO/TA System; Regatta Lateral System; Explorer TO System; WaveForm C Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; FORZA XP Expandable Spacer System; Shoreline ACS Interbody System; Shoreline RT Interbody System; Merid Orthofix Medical Inc.


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