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Orthofix Medical, Inc.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2024-06-20
TypeNumberDevice NameCodeDate
510(k) K240830 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; Meridian Interbody System; WaveForm A Interbody System MAX 2024-06-20 View