FDA Clears Sculptor Robotic Guidance Arm™ for Unicompartmental Knee Replacement Surgery (via PR Newswire)
LONDON, Feb. 5, 2013 /PRNewswire/ — Stanmore Implants (‘Stanmore’), specialists in the design and manufacture of patient specific and modular orthopaedic implants, announced today that it has received 510(k) clearance from the US Food and Drug Administration (FDA) to market its Sculptor Robotic Guidance…
published: February 6, 2013 in: Approval/Clearance, Knee, Technology