FDA 510(k) Applications Submitted by ROBERT COMPTON

FDA 510(k) Number Submission Date Device Name Applicant
K170318 02/01/2017 NeoFuse Ti3D PLIF/TLIF/Cervical Interbody HT Medical, LLC
K170511 02/21/2017 NeoFuse HA Enhanced PLIF/TLIF HT Medical, LLC
K170855 03/22/2017 T-Rex Standalone ALIF SIATS, LLC
K211496 05/13/2021 TransLoc 3D Foundation Fusion Solutions, LLC (dba CornerLoc)
K153615 12/17/2015 NeoFuse HA Enhanced PLIF/TLIF HT MEDICAL, LLC


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