FDA 510(k) Applications Submitted by Bruce Dunaway

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180090	01/12/2018	CureÖ Lumbar Plate System	Meditech Spine, LLC
K210286	02/02/2021	Cure 2.0 Anterior Cervical Plate (ACP) System	Meditech Spine, LLC
K170395	02/08/2017	Talos« Lumbar (HA) PEEK IBF Devices	Meditech Spine, LLC
K160604	03/02/2016	CureÖ Anterior Cervical Plate (ACP) System	MEDITECH SPINE, LLC
K201136	04/28/2020	CureÖ Lumbar Plate System	Meditech Spine, LLC
K171538	05/26/2017	CureÖ Lumbar Plate System	Meditech Spine, LLC
K201506	06/05/2020	Talos«-C Cervical Intervertebral Body Fusion System, Talos«-C (HA) Cervical Intervertebral Body Fusion System	Meditech Spine, LLC
K181543	06/12/2018	CureÖ OPEL-C Plate System	Meditech Spine, LLC