Class Class II
Argo Knotless GENESYS Anchor (K244025)
Description
Argo Knotless GENESYS Anchor by Conmed Corporation, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK244025
Clearance Date2025-01-28
Clearance TypeSpecial
Product CodeMBI
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K244025
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Argo Knotless GENESYS Anchor (K244025) cites 1 predicate device and is itself cited by 2 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240090 | Argo Knotless GENESYS Anchor | Conmed Corporation | 2024 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251296 | The Acumed Wrist Fixation System | Acumed, LLC | 2025 |
| K251530 | CONMED Argo Knotless® Anchor | Conmed Corporation | 2025 |
Trace the full predicate network for K244025
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.