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THINK Surgical Receives FDA 510(k) Clearance for Zimmer Biomet Persona Knee on TMINI® Miniature Robotic System

TMINI Miniature Robotic System

THINK Surgical, Inc. has announced that its TMINI® Miniature Robotic System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use with the Persona® The Personalized Knee System® from Zimmer Biomet.

The availability of the Persona Knee System on an exclusive version of the TMINI System is a major milestone for THINK Surgical. THINK Surgical is the only company offering a robotic system providing both an implant exclusive option with the Persona Knee System and an open implant platform for use with implants from multiple other manufacturers for total knee arthroplasty.

This go-to-market strategy supports two distinct customer segments, one which prefers an open platform where the customer can choose from a range of implants on the robot and another which prefers an exclusive platform with the market leading Persona Knee System.

“TMINI addresses surgeon demand for ergonomic, wireless, handheld robotic systems and we believe this will accelerate adoption of robotics in knee procedures, particularly in the out-patient setting.” said THINK Surgical CEO, Stuart Simpson.

Source: THINK Surgical, Inc.

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