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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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