Argo Knotless GENESYS Anchor
K-Number: K240090 · 2024-03-05
ApplicantConmed Corporation
Decision Date2024-03-05
Product CodeMAI
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 2024-03-05 under approval number K240090. The device is classified under product code MAI. 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 2024-03-05. It is manufactured by Conmed Corporation. The 510(k) number is K240090.
When was Argo Knotless GENESYS Anchor approved by the FDA?
Argo Knotless GENESYS Anchor received FDA 510(k) clearance on 2024-03-05, under approval number K240090.
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 MAI.
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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.