KFx Medical Receives FDA 510(k) Clearance for Tissue Fixation Anchor

KFx Medical Corp. has announced it has received FDA 510(k) clearance for its 5mm AppianFx tissue fixation anchor, according to a news release.

 

The AppianFx line of implants from KFx reattach tissue to bone in shoulder, knee, foot and ankle procedures

 

"This new anchor enables KFx to expand into the rapidly growing foot and ankle repair and reconstruction market, as well as other applications requiring smaller implants," said Tate Scott, president and CEO of KFx Medical, in the release. "While the AppianFx family of implants is successfully being adopted by orthopedic surgeons for a variety of repair and reconstruction procedures in the shoulder and knee, we are excited about offering foot and ankle surgeons anchors for small joint procedures and the early customer feedback has been nothing short of remarkable."

 

KFx Medical Corp. is headquartered in Carlsbad, Calif.

 

Related Articles on FDA Clearances:

Siemens Receives FDA Clearance for Perspective CT Scanner

Toshiba Receives FDA Clearance for ENCORE VeloCT Console

Cochlear Americas Receives FDA Approval of Electrode for Cochlear Implantation

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Articles We Think You'll Like

 

Featured Whitepapers

Featured Webinars