Argo Knotless GENESYS Anchor
K-Number: K244025 · 2025-01-28
ApplicantConmed Corporation
Decision Date2025-01-28
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Argo Knotless GENESYS Anchor is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2025-01-28 under approval number K244025. 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 GENESYS Anchor?
Argo Knotless GENESYS Anchor is a medical device that received FDA 510(k) clearance on 2025-01-28. It is manufactured by Conmed Corporation. The 510(k) number is K244025.
When was Argo Knotless GENESYS Anchor approved by the FDA?
Argo Knotless GENESYS Anchor received FDA 510(k) clearance on 2025-01-28, under approval number K244025.
What company makes Argo Knotless GENESYS Anchor?
Argo Knotless GENESYS Anchor is manufactured by Conmed Corporation.
What is the FDA product code for Argo Knotless GENESYS Anchor?
The FDA product code for Argo Knotless GENESYS 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.