{"id":"0f6edf60-ab96-4709-8c25-f47c0ae39677","slug":"fda-k242373-stryker-mako-shoulder","filingNumber":"K242373","filingType":"fda_510k","jurisdiction":"us_fda","applicantCompanyId":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","filingDate":"2024-08-09T12:00:00.000Z","decisionDate":"2024-11-07T12:00:00.000Z","status":"cleared","clearanceScope":"510(k) clearance for the Stryker Mako Shoulder application; cleared 2024.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242373","title":"FDA 510(k) K242373 - Stryker Mako Shoulder","sourceName":"FDA 510(k) Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:12.039Z","updatedAt":"2026-06-05T15:35:48.664Z","applicantCompany":{"id":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","slug":"stryker","name":"Stryker"},"modelLinks":[{"id":"f697ae8b-6bde-402a-92dc-176b4a84ccc1","modelId":"b3a006a0-d844-4fb4-b4d9-dd6f148c0958","regulatoryFilingId":"0f6edf60-ab96-4709-8c25-f47c0ae39677","createdAt":"2026-06-04T23:17:12.195Z","model":{"slug":"stryker-mako","modelName":"Mako"}}]}