THINK Surgical receives US FDA 510(k) clearance for its TMINI miniature robotic system

29th August, 2024

For use with the GMK Sphere and SpheriKA Knee Systems from Medacta International

image credit- shutterstock

image credit- shutterstock

THINK Surgical announced that its TMINI miniature robotic system has received 510(k) clearance from the U.S. FDA for use with the GMK Sphere and SpheriKA Knee Systems from Medacta International under a collaboration Agreement between the two companies.

The GMK Sphere and SpheriKA Knee Systems have been added to THINK Surgical's ID-HUB, a proprietary data bank of implant modules for use with the open platform version of its TMINI System.

The GMK Sphere implant, a ball-in-socket knee design, and the SpheriKA implant, the world's first knee system specifically designed based on the principles of Kinematic Alignment, add to THINK Surgical's ID HUB database. This addition will allow Medacta customers access to robotic-assisted technology for total knee replacement in the United States.  

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