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Devices · THINK Surgical, Inc.

TMINI Miniature Robotic System

510(k)K250877NeurologyOLO

THINK Surgical, Inc. is listed for TMINI Miniature Robotic System (K250877). The FDA list gives June 20, 2025 as the date of the final decision. The lead panel is Neurology, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code OLO as “Orthopedic Stereotaxic Instrument”: Stereotaxic guidance during orthopedic surgery procedures. Indicated for Orthopedic joint or spine surgery. Neurological stereotaxic instruments are classified under product code HAW. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K250877

Official FDA database record

Date of final decision
June 20, 2025
Company on the FDA list
THINK Surgical, Inc.
Lead panel
Neurology
Primary product code
OLO
openFDA device name for the code
Orthopedic Stereotaxic Instrument
Device class
2
Regulation number
882.4560
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

Stereotaxic guidance during orthopedic surgery procedures. Indicated for Orthopedic joint or spine surgery. Neurological stereotaxic instruments are classified under product code HAW.

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