Zimmer’s Personalised Knee Replacement Gets FDA Clearance

Zimmer has received FDA 510(k) clearance to market iASSIST™ Knee, the Personalized Guidance System™ for knee replacement procedures. Zimmer says its device provides simple, intuitive and accurate intraoperative feedback and alignment validation to surgeons during joint replacement procedures, eliminating the need for bulky capital equipment.



Zimmer Receives FDA Clearance for Revolutionary New Surgical Guidance Technology (via PR Newswire)

iASSIST™ Knee Supports Streamlined, Personalized Knee Replacement Procedures WARSAW, Ind., Jan. 17, 2013 /PRNewswire/ — Zimmer Holdings, Inc. (NYSE: ZMH; SIX: ZMH), a global leader in musculoskeletal health, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration…



published: January 21, 2013 in: Approval/Clearance, Knee, Zimmer

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