Extremity Medical Receives FDA 510(k) Clearance for Axis Charcot Fixation

Extremity Medical announced FDA 510(k) clearance for Axis Charcot, a comprehensive axial fixation system. First cases are scheduled for this month.

This product and the recently-released BioFuse next-gen live-cell bone graft are two of the company's 16...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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