FDA 510(k) Applications Submitted by Osseus Fusion Systems, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K131810 06/19/2013 OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM OSSEUS FUSION SYSTEMS, LLC
K213590 11/12/2021 Blue Topaz Sacroiliac Screw System Osseus Fusion Systems, LLC
K160522 02/25/2016 White Pearl Preferred Angle Anterior Cervical Plate OSSEUS FUSION SYSTEMS, LLC
K170844 03/21/2017 Gemini-C Hybrid Cervical Interbody System Osseus Fusion Systems, LLC
K181347 05/21/2018 Aries« Lumbar Interbodies Osseus Fusion Systems, LLC


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