{"id":"945963dc-697e-42ba-84eb-0f9e542ba3b6","slug":"momentis-anovo-fda-510k","filingNumber":null,"filingType":"fda_510k","jurisdiction":"us_fda","applicantCompanyId":null,"filingDate":null,"decisionDate":"2026-06-01T00:00:00.000Z","status":"cleared","clearanceScope":"Momentis Surgical ANOVO second-generation robotic platform FDA 510(k) clearance. First approval was De Novo authorization.","sources":[{"url":"https://www.surgicalroboticstechnology.com/news/momentis-surgical-receives-fda-510k-clearance-for-second-generation-anovo-robotic-platform/","title":"Momentis Surgical ANOVO FDA 510(k)"}],"verificationPosture":null,"capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"unreviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-07-18T12:44:07.067Z","updatedAt":"2026-07-18T12:44:07.067Z","applicantCompany":null,"modelLinks":[{"id":"4e159bea-0311-45d9-a60d-3073c47dbc8b","modelId":"1b6216e1-4bc9-4e82-9185-67b1117341d6","regulatoryFilingId":"945963dc-697e-42ba-84eb-0f9e542ba3b6","createdAt":"2026-07-18T12:44:07.452Z","model":{"slug":"momentis-anovo","modelName":"ANOVO"}}]}