Meditech Spine, LLC
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories3
Latest Approval2021-03-18
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K210286 | Cure 2.0 Anterior Cervical Plate (ACP) System | KWQ | 2021-03-18 | View |
| 510(k) | K201506 | Talos®-C Cervical Intervertebral Body Fusion System, Talos®-C (HA) Cervical Intervertebral Body Fusion System | ODP | 2020-09-11 | View |
| 510(k) | K201136 | Cure Lumbar Plate System | KWQ | 2020-05-12 | View |
| 510(k) | K181543 | Cure OPEL-C Plate System | KWQ | 2018-08-31 | View |
| 510(k) | K180090 | Cure Lumbar Plate System | KWQ | 2018-04-23 | View |
| 510(k) | K171538 | Cure Lumbar Plate System | KWQ | 2017-06-16 | View |
| 510(k) | K170395 | Talos® Lumbar (HA) PEEK IBF Devices | MAX | 2017-06-02 | View |
| 510(k) | K160604 | Cure Anterior Cervical Plate (ACP) System | KWQ | 2016-07-01 | View |
No matching devices.