CONMED Argo Knotless® Anchor
K-Number: K251530 · 2025-06-18
ApplicantConmed Corporation
Decision Date2025-06-18
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CONMED Argo Knotless® Anchor is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2025-06-18 under approval number K251530. 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 CONMED Argo Knotless® Anchor?
CONMED Argo Knotless® Anchor is a medical device that received FDA 510(k) clearance on 2025-06-18. It is manufactured by Conmed Corporation. The 510(k) number is K251530.
When was CONMED Argo Knotless® Anchor approved by the FDA?
CONMED Argo Knotless® Anchor received FDA 510(k) clearance on 2025-06-18, under approval number K251530.
What company makes CONMED Argo Knotless® Anchor?
CONMED Argo Knotless® Anchor is manufactured by Conmed Corporation.
What is the FDA product code for CONMED Argo Knotless® Anchor?
The FDA product code for CONMED Argo Knotless® 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.