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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