Extremity Medical Receives 510(k) FDA Clearance for HammerFiX Device

Extremity Medical announced that it has received 510(k) clearance from the U.S. Food and Drug Administration for the HammerFiX device.

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The device is indicated for the fixation of osteotomies and reconstruction of the lesser toes following correction procedures for hammertoe, claw toe and mallet toe. It was designed for stability and maintenance of the correction.   

 

Extremity Medical is an orthopedic device company focusing on the development of next generation systems.

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