Cleared Traditional

TMINI Miniature Robotic System (TMINI 1.1)

K241031 · THINK Surgical, Inc. · Orthopedic

Jul 2024

Decision

88d

Days

Class 2

Risk

About This 510(k) Submission

K241031 is an FDA 510(k) clearance for the TMINI Miniature Robotic System (TMINI 1.1), 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 July 12, 2024, 88 days after receiving the submission on April 15, 2024. This device falls under the Orthopedic review panel. Regulated under 21 CFR 882.4560.

Submission Details

510(k) Number	K241031 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 15, 2024
Decision Date	July 12, 2024
Days to Decision	88 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.