Think Surgical receives FDA 510(k) clearance for new software in robotic TKA system

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Think Surgical Inc. announced FDA clearance of the TMINI 1.1 miniature robotic system.
The clearance includes updated surgical workflow software.

Think Surgical Inc. announced it received FDA 510(k) clearance for the TMINI 1.1 miniature robotic system, a new software system for the TMINI robotic knee replacement platform, according to a company press release.

The TMINI 1.1 system is designed with updated workflow software for surgical planning and intraoperative performance, according to the release.

Generic FDA News infographic — Think Surgical announced FDA clearance of the TMINI 1.1 miniature robotic system.

“This software release is a major enhancement to our TMINI robotic system that not only meets our customers’ needs but is a differentiator for our platform in this industry,” Stuart Simpson, president and CEO of Think Surgical, said in the release. “It is a major accomplishment for our company to receive a second FDA clearance for our TMINI system in less than 15 months. This demonstrates our development capabilities and commitment to innovation as a focused robotics and digital surgery company.”

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Think Surgical receives FDA 510(k) clearance for new software in robotic TKA system

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