Stryker Corp. announced 510(k) clearance of its Mako robotic surgical platform for a total knee replacement indication Aug. 6. The total knee application is the biggest market opportunity for the robotic device, which is already cleared for partial knee and total hip replacements, according to the firm. (See Also see "FDA Clears Stryker's Mako Robot To Treat Total Hip Replacement" - Medtech Insight, 25 March, 2015..) But a need for training and necessary software upgrades to installed systems will hold off an immediate launch of the total knee application, which will employ Stryker's Triathlon knee implant. The company is preparing for a limited market release by year end. The Mako system consists of a robotic arm that guides a surgeon through a procedure.
Apollo Endosurgery Inc. is second to the U.S. market with an intragastric balloon for obesity with the Aug. 5 FDA approval
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