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FDA 510(k)

NavLock Trackers

K-Number: K201327 · 2020-06-18

ApplicantMedtronic Navigation
Decision Date2020-06-18
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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