Cleared Traditional

TMINI? Miniature Robotic System

K260010 · THINK Surgical, Inc. · Orthopedic

Mar 2026

Decision

60d

Days

Class 2

Risk

About This 510(k) Submission

K260010 is an FDA 510(k) clearance for the TMINI? Miniature Robotic System, a Orthopedic Stereotaxic Instrument (Class II — Special Controls, product code OLO), submitted by THINK Surgical, Inc. (Fremont, US). The FDA issued a Cleared decision on March 3, 2026, 60 days after receiving the submission on January 2, 2026. This device falls under the Orthopedic review panel. Regulated under 21 CFR 882.4560.

Submission Details

510(k) Number	K260010 FDA.gov
FDA Decision	Cleared SESE
Date Received	January 02, 2026
Decision Date	March 03, 2026
Days to Decision	60 days
Submission Type	Traditional
Review Panel	Orthopedic (OR)
Summary	Summary PDF

Device Classification

Product Code	OLO — Orthopedic Stereotaxic Instrument
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 882.4560
Definition	Stereotaxic Guidance During Orthopedic Surgery Procedures. Indicated For Orthopedic Joint Or Spine Surgery. Neurological Stereotaxic Instruments Are Classified Under Product Code Haw.