Meditech Spine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meditech Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Cure 2.0 Anterior Cervical Plate (ACP) System, Talos®-C Cervical Intervertebral Body Fusion System, Talos®-C (HA) Cervical Intervertebral Body Fusion System, Cure™ Lumbar Plate System
10
Total
10
Cleared
0
Denied
Meditech Spine, LLC has 10 FDA 510(k) cleared orthopedic devices. Based in Atlanta, US.
Last cleared in 2021. Active since 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meditech Spine, LLC
10 devices
Cleared
Mar 18, 2021
Cure 2.0 Anterior Cervical Plate (ACP) System
Orthopedic
44d
Cleared
Sep 11, 2020
Talos®-C Cervical Intervertebral Body Fusion System, Talos®-C (HA) Cervical...
Orthopedic
98d
Cleared
May 12, 2020
Cure™ Lumbar Plate System
Orthopedic
14d
Cleared
Aug 31, 2018
Cure™ OPEL-C Plate System
Orthopedic
80d
Cleared
Apr 23, 2018
Cure™ Lumbar Plate System
Orthopedic
101d
Cleared
Jun 16, 2017
Cure™ Lumbar Plate System
Orthopedic
21d
Cleared
Jun 02, 2017
Talos® Lumbar (HA) PEEK IBF Devices
Orthopedic
114d
Cleared
Jul 01, 2016
Cure™ Anterior Cervical Plate (ACP) System
Orthopedic
121d
Cleared
Oct 14, 2015
Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral...
Orthopedic
203d
Cleared
Feb 22, 2015
Talos-C(HA) Cervical Intervertebral Body Fusion Devices
Orthopedic
184d