FDA
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Orthofix International (OFIX) Receives 510(k) Clearance and CE Mark for TrueLok Elevate Transverse Bone Transport System
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Orthofix Announces Publication of New Data Supporting Use of PEMF Stimulation in Lumbar Spine Fusion Procedures for Patients at Risk of Pseudarthrosis
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Orthofix and SeaSpine to Combine in Merger of Equals to Create Leading Global Spine and Orthopedics Company
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Orthofix International (OFIX) Granted FDA PMA for the AccelStim Bone Growth Stimulation Device
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Orthofix Announces First US Pediatric Implant of the Fitbone Limb-Lengthening System
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Orthofix Reports First Quarter 2021 Results
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Orthofix Announces Publication of Two-Year Data from the M6-C Artificial Cervical Disc Study
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