Flow-Fx's Flow-Screw Wins FDA Approval

Mokena, Ill., Mar. 24, 2015 /PRNewswire-iReach/ -- Flow-FX LLC announced today that the FDA has allowed 510K clearance for its Flow-Screw product family. Flow-Screw is approved for fixation of bone fractures as well as allowing injectable bone void filler delivery to a surgical site. Size ranges from 3.5mm to 7.3 mm and will be manufactured in titanium alloy.

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Flow-Screw is the second product family cleared by the FDA as the Flow-Nail was cleared in July, 2014. Its patented screw/cannula system enables precision delivery of bone void filler through a cannulated screw.

Flow-FX continues to meet its milestones, receiving ISO 13485 certification in March 2015 and entering production on both 2-CAN and Flow-Nail for second quarter release.

Flow-FX LLC remains ambitious in their long term goals. "The future of complex orthopedic trauma is through fixation devices that facilitate biologic delivery. Our devices open the door for the next generation of advances in orthopedic healthcare" stated Patrick Sweeney MD, the company's founder. 

For more about Flow-FX visit www.Flow-FX.net or booth 3808 at the AAOS meeting, Las Vegas3/25-3/27/2015

Media Contact:Patrick Sweeney, Flow-Fx LLc, 8155314424, p.sweeney@Flow-Fx.net

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SOURCE Flow-Fx LLc