FDA 510(k)

Intellijoint VIEW

K号: K211876 · 2021-11-12

决定日期2021-11-12

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

Intellijoint VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2021-11-12 under 510(k) number K211876. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Intellijoint VIEW?

Intellijoint VIEW is a medical device that received FDA 510(k) clearance on 2021-11-12. The listed applicant is Intellijoint Surgical, Inc.. The 510(k) number is K211876.

When did Intellijoint VIEW receive FDA 510(k) clearance?

Intellijoint VIEW received FDA 510(k) clearance on 2021-11-12, under 510(k) number K211876.

Who is the listed applicant for Intellijoint VIEW?

The FDA 510(k) record lists Intellijoint Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intellijoint VIEW?

The FDA product code for Intellijoint VIEW is LLZ.

列明Intellijoint 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。

K191507Intellijoint® 导航系统 K172849Intellijoint HIP 系统 K171525Intellijoint HIP 系统（车用），Intellijoint HIP 系统（便携式），Intellijoint HIP 仪器托盘 K162364Intellijoint HIP 2A 系统

官方来源

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