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FDA 510(k)

LOCATOR F-Tx Attachment System

K-Number: K151789 · 2016-03-04

ApplicantZest Anchors, LLC
Decision Date2016-03-04
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOCATOR F-Tx Attachment System is a medical device manufactured by Zest Anchors, LLC. It received FDA 510(k) clearance on 2016-03-04 under approval number K151789. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCATOR F-Tx Attachment System?

LOCATOR F-Tx Attachment System is a medical device that received FDA 510(k) clearance on 2016-03-04. It is manufactured by Zest Anchors, LLC. The 510(k) number is K151789.

When was LOCATOR F-Tx Attachment System approved by the FDA?

LOCATOR F-Tx Attachment System received FDA 510(k) clearance on 2016-03-04, under approval number K151789.

What company makes LOCATOR F-Tx Attachment System?

LOCATOR F-Tx Attachment System is manufactured by Zest Anchors, LLC.

What is the FDA product code for LOCATOR F-Tx Attachment System?

The FDA product code for LOCATOR F-Tx Attachment System is NHA.

Related Clinical Trials

NCT07526818 Comparison of Manual and Mechanical Glide Path Techniques for Measuring Root Canal Length Using Standalone Apex Locator and an Endomotor With built-in Apex Locator. ACTIVE_NOT_RECRUITING

Other Devices by Zest Anchors, LLC

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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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