Class Class II
NextStep Arthropedix Total Knee System (K242410)
Description
NextStep Arthropedix Total Knee System by Nextstep Arthropedix, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242410
Clearance Date2025-05-08
Clearance TypeTraditional
Product CodeJWH
Regulation Number888.3560
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242410
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. NextStep Arthropedix Total Knee System (K242410) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221479 | Persona Personalized Knee System | Zimmer, Inc. | 2022 |
| K202022 | GMK-SPHERE Tibial inserts FLEX Tibial Insert CR and Resurfa... | Medacta International S.A. | 2020 |
| K150783 | Progressive Orthopaedic Total Knee System | The Progressive Orthopaedic Company... | 2015 |
| K142649 | Progressive Orthopedic Total Knee System | The Progressive Orthopaedic Company... | 2015 |
| K121416 | GMK SPHERE | Medacta International | 2012 |
Trace the full predicate network for K242410
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.