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FDA 510(k) Applications Submitted by Atlas Spine, Inc.
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.
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