Class Class II

TMINI™ Miniature Robotic System (K230202)

K230202 2023-04-25 Traditional
Home/ Devices/ TMINI™ Miniature Robotic System…

Description

TMINI™ Miniature Robotic System by THINK Surgical, Inc. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230202
Clearance Date2023-04-25
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top