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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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