Class Class II

Evolution® Total Knee Systems – Kinematic Alignment Instrumentation and Technique (K243574)

K243574 2025-02-18 Traditional
Home/ Devices/ Evolution® Total Knee Systems…

Description

Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique by Microport Orthopedics, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243574
Clearance Date2025-02-18
Clearance TypeTraditional
Product CodeJWH
Regulation Number888.3560

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote

Predicate lineage for K243574

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. Evolution® Total Knee Systems – Kinematic Alignment Instrumentation and Technique (K243574) cites 4 predicate devices and is itself cited by 1 later device.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K152298EVOLUTION BIOFOAM Tibial Base, EVOLUTION Modular Keels, ADV...Microport Orthopedics, Inc.2015
K140735EVOLUTION MP CS/CR POROUS FEMUR/EVOLUTION ADAPTIVE CS AND P...Microport Orthopedics, Inc.2014
K102380EVOLUTION MP TOTAL KNEE SYSTEMWrightmedicaltechnologyinc2011
K093552EVOLUTION MP TOTAL KNEE SYSTEMWrightmedicaltechnologyinc2010

Later devices that cite this one as their predicate

Devices that cite K243574
K numberDeviceApplicantYear
K253728EVOLUTION® AM BIOFOAM® Tibial SystemMicroport Orthopedics, Inc.2026

Trace the full predicate network for K243574

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.

Scroll to Top