Orthofix received FDA 510(k) clearance to market the G-Beam™ Fusion Beaming system, designed to provide alignment, stabilization and fixation to treat neuropathic deformities such as Charcot foot.
G-Beam is accompanied by single-use, sterile-packed implants and a compact instrumentation tray. The system supports the company’s strategy to be a premium provider for Charcot and diabetic foot markets.
Source: Orthofix International N.V.

Image courtesy of Orthofix International N.V.
Orthofix received FDA 510(k) clearance to market the G-Beam™ Fusion Beaming system, designed to provide alignment, stabilization and fixation to treat neuropathic deformities such as Charcot foot.
G-Beam is accompanied by single-use, sterile-packed implants and a compact instrumentation tray. The system supports the company's strategy to be a...
Orthofix received FDA 510(k) clearance to market the G-Beam™ Fusion Beaming system, designed to provide alignment, stabilization and fixation to treat neuropathic deformities such as Charcot foot.
G-Beam is accompanied by single-use, sterile-packed implants and a compact instrumentation tray. The system supports the company’s strategy to be a premium provider for Charcot and diabetic foot markets.
Source: Orthofix International N.V.

Image courtesy of Orthofix International N.V.
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JV
Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.





