FDA 510(k) Applications Submitted by Robert Pace

FDA 510(k) Number Submission Date Device Name Applicant
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
K192121 08/06/2019 Black Diamond Pedicle Screw System Osseus Fusion Systems
K192495 09/11/2019 Black Diamond Navigation Instruments Osseus Fusion Systems


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