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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
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