{"url_path":"/fda/devices/510k/K261624","section_key":"summary","section_title":"510(k) Clearance: Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Inser…","topic":"fda","document":{"doc_type":"510k-clearance","doc_date":"2026-07-10","source_url":"https://api.fda.gov/device/510k.json?search=k_number:%22K261624%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Howmedica Osteonics Corp., Dba Stryker Orthopaedics"},"word_count":84,"has_tables":false,"body_markdown":null}