FDA 510(k)

Argo Knotless SP Anchor

K-Number: K220757 · 2022-05-13

Decision Date2022-05-13

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Argo Knotless SP Anchor is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2022-05-13 under approval number K220757. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Argo Knotless SP Anchor?

Argo Knotless SP Anchor is a medical device that received FDA 510(k) clearance on 2022-05-13. It is manufactured by Conmed Corporation. The 510(k) number is K220757.

When was Argo Knotless SP Anchor approved by the FDA?

Argo Knotless SP Anchor received FDA 510(k) clearance on 2022-05-13, under approval number K220757.

What company makes Argo Knotless SP Anchor?

Argo Knotless SP Anchor is manufactured by Conmed Corporation.

What is the FDA product code for Argo Knotless SP Anchor?

The FDA product code for Argo Knotless SP Anchor is MBI.

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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.