FDA 510(k) Applications Submitted by MEDITECH SPINE, LLC
| 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 |
| K150788 |
03/25/2015 |
Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral Body Fusion Devices, Talos -C(HA) Cervical Intervertebral Body Fusion Devices |
MEDITECH SPINE, LLC |
| K142345 |
08/22/2014 |
Talos-C(HA) Cervical Intervertebral Body Fusion Devices |
MEDITECH SPINE, LLC |
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