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Osseus Fusion Systems, LLC

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories4
Latest FDA decision2022-03-01
TypeNumberDevice NameCodeDateActions
510(k) K213590 Blue Topaz Sacroiliac Screw SystemOUR2022-03-01 View
510(k) K181347 Aries® Lumbar InterbodiesMAX2018-08-15 View
510(k) K170844 Gemini-C Hybrid Cervical Interbody SystemODP2017-07-03 View
510(k) K160522 White Pearl Preferred Angle Anterior Cervical PlateKWQ2016-04-26 View
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