Class Class II
MagnetOs MIS (K243474)
Description
MagnetOs MIS by Kuros Biosciences B.V, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243474
Clearance Date2025-05-23
Clearance TypeTraditional
Product CodeMQV
Regulation Number888.3045
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243474
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. MagnetOs MIS (K243474) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K242299 | NovaBone Putty - Synthetic Bioactive Bone Graft | Novabone Products, LLC | 2024 |
| K241212 | MagnetOs Easypack Putty | Kuros Biosciences | 2024 |
| K240442 | MagnetOs Putty | Kuros Biosciences B.V | 2024 |
Trace the full predicate network for K243474
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.