FDA 510(k)

TMINI®微型机器人系统

K号: K260010 · 2026-03-03

决定日期2026-03-03

产品代码OLO

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决定实质等同

器械摘要

TMINI® Miniature Robotic System is the device name listed in this FDA 510(k) record. The listed applicant is THINK Surgical, Inc.. It received FDA 510(k) clearance on 2026-03-03 under 510(k) number K260010. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TMINI® Miniature Robotic System?

TMINI® Miniature Robotic System is a medical device that received FDA 510(k) clearance on 2026-03-03. The listed applicant is THINK Surgical, Inc.. The 510(k) number is K260010.

When did TMINI® Miniature Robotic System receive FDA 510(k) clearance?

TMINI® Miniature Robotic System received FDA 510(k) clearance on 2026-03-03, under 510(k) number K260010.

Who is the listed applicant for TMINI® Miniature Robotic System?

FDA 510(k)记录中列出了THINK Surgical, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for TMINI® Miniature Robotic System?

The FDA product code for TMINI® Miniature Robotic System is OLO.

列明THINK Surgical, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K261024TMINI微型机器人系统 K253661TMINI微型机器人系统 K252544TMINI微型机器人系统 K250877TMINI微型机器人系统 K243481TMINI微型机器人系统 K243285TMINI微型机器人系统

查看所有 22 个设备 →

官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。