{"id":"1ad00c66-3361-4d19-b0c7-0dba0d40f06f","slug":"fda-510k-mako-tgs-2008","filingNumber":"K072806","filingType":"fda_510k","jurisdiction":"us_fda","applicantCompanyId":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","filingDate":"2007-10-01T12:00:00.000Z","decisionDate":"2008-01-24T12:00:00.000Z","status":"cleared","clearanceScope":"Foundational FDA 510(k) clearance of the MAKO Tactile Guidance System (TGS), the robotic-arm orthopedic platform underpinning Mako/RIO; filed by MAKO Surgical Corp. (acquired by Stryker in 2013).","sources":[{"url":"https://api.fda.gov/device/510k.json?search=k_number:K072806","title":"FDA 510(k) K072806","sourceName":"openFDA (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-05T19:02:09.999Z","updatedAt":"2026-06-05T19:02:09.999Z","applicantCompany":{"id":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","slug":"stryker","name":"Stryker"},"modelLinks":[{"id":"043f3056-6448-47d5-818f-c24200d75979","modelId":"b3a006a0-d844-4fb4-b4d9-dd6f148c0958","regulatoryFilingId":"1ad00c66-3361-4d19-b0c7-0dba0d40f06f","createdAt":"2026-06-05T19:02:10.079Z","model":{"slug":"stryker-mako","modelName":"Mako"}}]}