FDA 510(k)

NavLock Trackers

K号: K201327 · 2020-06-18

决定日期2020-06-18

产品代码OLO

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决定实质等同

器械摘要

NavLock Trackers is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Navigation. It received FDA 510(k) clearance on 2020-06-18 under 510(k) number K201327. 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 NavLock Trackers?

NavLock Trackers is a medical device that received FDA 510(k) clearance on 2020-06-18. The listed applicant is Medtronic Navigation. The 510(k) number is K201327.

When did NavLock Trackers receive FDA 510(k) clearance?

NavLock Trackers received FDA 510(k) clearance on 2020-06-18, under 510(k) number K201327.

Who is the listed applicant for NavLock Trackers?

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

What is the FDA product code for NavLock Trackers?

The FDA product code for NavLock Trackers is OLO.

列明Medtronic Navigation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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