FDA Clears Exactech’s TriVerse Primary Knee System

Exactech’s TriVerse primary knee system has gained 510(k) clearance from the FDA for knee replacements.

The system contains insert bearings with vitamin E-stabilized polyethylene — which prevent oxidation and enhance long-term performance — and includes cruciate retaining and anterior stabilized and posterior stabilized components.

The system includes a compact set of adjustable instrumentation with future compatibility with its ExactechGPS (guided personalized surgery) system, the company said.

Exactech plans a limited launch of TriVerse in the second quarter of 2023.