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EVOLUTION® Hinge Knee System - EVOLUTION® Hinge Knee System

by MicroPort Orthopedics Inc. 510(k)

Active United States

510(k) K240043

Overview

The Evolution and Advance Knee Systems are modular orthopedic implants designed for total knee arthroplasty, revision surgery, and limb salvage procedures. These systems include hinge knee designs, modular distal femoral components, and customizable tibial inserts to address complex joint pathologies, such as severe osteoarthritis, post-traumatic deformities, or oncologic reconstructions. The Repiphysis and Guardian systems specifically target limb salvage applications, providing structural support and stability for patients requiring extensive bone resection or tumor removal. Inserts such as the Adaptive CS, PS, and Ultra-Congruent variants are engineered to optimize joint congruency and load distribution, enhancing long-term durability and patient mobility.

These devices are intended for use in orthopedic operating rooms by trained surgeons and are supplied sterile for single-use. The modular components allow for customization based on patient anatomy and clinical needs, with sizes and configurations detailed in the manufacturer’s technical documentation. The Evolution and Advance systems are classified under FDA 510(k) clearance (K240043) as substantially equivalent to predicate devices, adhering to traditional review pathways. Storage and handling follow standard orthopedic implant protocols to maintain sterility and integrity prior to surgical use.

AI-generated from registry data, 18 Sep 2026.Not verified by deviCERTS or the manufacturer

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK240043 Date1 Apr 2024ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 25 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KRO
FDA applicant
Microport Orthopedics, Inc.
Device Class
Class II
Regulation
21 CFR Part 888.3510
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

From the manufacturer

Manufacturer's product page: Evolution® Kinematic Alignment

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