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FDA 510(k)

High Retention Attachment System

K-Number: K220252 · 2022-04-14

ApplicantZest Anchors, LLC
Decision Date2022-04-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

High Retention Attachment System is a medical device manufactured by Zest Anchors, LLC. It received FDA 510(k) clearance on 2022-04-14 under approval number K220252. 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 High Retention Attachment System?

High Retention Attachment System is a medical device that received FDA 510(k) clearance on 2022-04-14. It is manufactured by Zest Anchors, LLC. The 510(k) number is K220252.

When was High Retention Attachment System approved by the FDA?

High Retention Attachment System received FDA 510(k) clearance on 2022-04-14, under approval number K220252.

What company makes High Retention Attachment System?

High Retention Attachment System is manufactured by Zest Anchors, LLC.

What is the FDA product code for High Retention Attachment System?

The FDA product code for High Retention Attachment System is NHA.

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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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