FDA 510(k) Applications Submitted by Thomas Smith

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180675	03/15/2018	Atlas Spine Expandable Cervical Interbody System	Atlas Spine, Inc.
K172334	08/02/2017	OrtusÖ Expandable Lumbar Interbody Fusion System	Atlas Spine, Inc.
K202302	08/14/2020	Atlas Spine Rebar (Ti) Spacer System	Atlas Spine, Inc.
K182418	09/05/2018	V3 Segmental Plating System	Atlas Spine, Inc.
K192570	09/18/2019	Atlas Spine Expandable Cervical Standalone Interbody System	Atlas Spine, Inc.
K162918	10/18/2016	Atlas Spine Expandable Interbody System	Atlas Spine, Inc.
K000443	02/10/2000	REMOTE FETAL MEDICINE ULTRASOUND SYSTEM	R4 TELEMEDICINE, INC.
K112759	09/22/2011	APCLO PEDICLE SCREW SYSTEMS	ATLAS SPINE INC.