{"id":"323cbd36-995e-4d72-921a-21601749dfbc","slug":"fda-k241517-stryker-mako-spine","filingNumber":"K241517","filingType":"fda_510k","jurisdiction":"us_fda","applicantCompanyId":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","filingDate":"2024-05-29T12:00:00.000Z","decisionDate":"2024-08-27T12:00:00.000Z","status":"cleared","clearanceScope":"510(k) clearance for the Stryker Mako Spine application; cleared 2024.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241517","title":"FDA 510(k) K241517 - Stryker Mako Spine","sourceName":"FDA 510(k) Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:11.430Z","updatedAt":"2026-06-05T15:35:48.431Z","applicantCompany":{"id":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","slug":"stryker","name":"Stryker"},"modelLinks":[{"id":"c6b94c66-59c8-4722-81da-972109e1d15d","modelId":"b3a006a0-d844-4fb4-b4d9-dd6f148c0958","regulatoryFilingId":"323cbd36-995e-4d72-921a-21601749dfbc","createdAt":"2026-06-04T23:17:11.736Z","model":{"slug":"stryker-mako","modelName":"Mako"}}]}