Class Class II
Activmotion S (K241539)
Description
Activmotion S by Newclip Technics, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241539
Clearance Date2024-07-30
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241539
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. Activmotion S (K241539) cites 3 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K173746 | Activmotion Range | Newclip Technics | 2018 |
| K141796 | DEPUY SYNTHES TOMOFIX OSTEOTOMY SYSTEM | Synthes (USA) Products, LLC | 2014 |
| K041601 | SURFIX KNEE OSTEOTOMY SYSTEM | Surfix Technologies | 2004 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K250155 | Xpert Knee | Newclip Technics | 2025 |
Trace the full predicate network for K241539
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.