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# Exactech’s TriVerse Knee System Cleared
- URL: https://www.fdaweb.com/exactechs-triverse-knee-system-cleared/
- Published: 2022-11-04T12:00:00.000Z
- Updated: 2026-09-14T18:05:12.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5153135

FDA has cleared an Exactech 510(k) for its TriVerse primary knee system. The device is designed to accommodate cruciate retaining, anterior stabilized and posterior stabilized constructs, according to the company. Its insert bearings are made of “highly crosslinked vitamin E-stabilized polyethylene,” it says, adding that it comes with a compact set of adjustable mechanical instrumentation. Eventually, Exactech says the knee system will be compatible with its [ExactechGPS](https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.exac.com%2Fknee%2Fexactechgps-knee-applications%2F&esheet=52960343&newsitemid=20221104005075&lan=en-US&anchor=ExactechGPS%26%23174%3B&index=2&md5=b4bd25d08c87ca5db769a9198731420e&ref=fdaweb.com) surgical navigation system.