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FDA 510(k)

LOCATOR Angled Abutment (Various)

K-Number: K233587 · 2024-06-03

ApplicantZest Anchors, LLC
Decision Date2024-06-03
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOCATOR Angled Abutment (Various) is a medical device manufactured by Zest Anchors, LLC. It received FDA 510(k) clearance on 2024-06-03 under approval number K233587. 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 Angled Abutment (Various)?

LOCATOR Angled Abutment (Various) is a medical device that received FDA 510(k) clearance on 2024-06-03. It is manufactured by Zest Anchors, LLC. The 510(k) number is K233587.

When was LOCATOR Angled Abutment (Various) approved by the FDA?

LOCATOR Angled Abutment (Various) received FDA 510(k) clearance on 2024-06-03, under approval number K233587.

What company makes LOCATOR Angled Abutment (Various)?

LOCATOR Angled Abutment (Various) is manufactured by Zest Anchors, LLC.

What is the FDA product code for LOCATOR Angled Abutment (Various)?

The FDA product code for LOCATOR Angled Abutment (Various) is NHA.

Related Clinical Trials

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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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