Class Class II
EVOS Pelvic and Acetabular System (K241666)
Description
EVOS Pelvic and Acetabular System by Smith & Nephew, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241666
Clearance Date2025-02-19
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241666
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. EVOS Pelvic and Acetabular System (K241666) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K173293 | EVOS Small Fragment Upper Extremity Plates | Smith & Nephew, Inc. | 2018 |
| K170887 | EVOS Small Fragment Plating System | Smith & Nephew, Inc. | 2017 |
| K162078 | EVOS Small Fragment Plating System | Smith & Nephew, Inc. | 2016 |
| K140814 | EVOS MINI-FRAGMENT PLATING SYSTEM | Smith & Nephew, Inc. | 2014 |
| K060736 | SMITH & NEPHEW 6.5MM AND 8.0MM CANNULATED SCREWS | Smith & Nephew, Inc. | 2006 |
Trace the full predicate network for K241666
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.