FDA 510(k)

CROSSNAV 导航启用工具用于椎间盘准备和椎间

K号: K254157 · 2026-05-26

决定日期2026-05-26

产品代码OLO

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决定实质等同

器械摘要

CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2026-05-26 under 510(k) number K254157. 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 CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody?

CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody is a medical device that received FDA 510(k) clearance on 2026-05-26. The listed applicant is Medos International SARL. The 510(k) number is K254157.

When did CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody receive FDA 510(k) clearance?

CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody received FDA 510(k) clearance on 2026-05-26, under 510(k) number K254157.

Who is the listed applicant for CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody?

The FDA 510(k) record lists Medos International SARL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody?

The FDA product code for CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody is OLO.

列明Medos International SARL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。

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