Corelink, LLC
FDA 510(k) & PMA Approved Dispositivos — 23 products
Publicidad
Total de dispositivos23
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K231743 | F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System | MAX | 2023-12-08 | Ver |
| 510(k) | K231494 | CoreLink Robotic Navigation Instruments | OLO | 2023-10-27 | Ver |
| 510(k) | K232116 | CoreLink Navigation Instruments | OLO | 2023-08-16 | Ver |
| 510(k) | K230329 | F3D Interbody System | ODP | 2023-06-06 | Ver |
| 510(k) | K230880 | CoreLink Navigation Instruments | OLO | 2023-05-02 | Ver |
| 510(k) | K223708 | Entasis 3D Dual-Lead Sacroiliac Implant System | OUR | 2023-03-21 | Ver |
| 510(k) | K221776 | NextGen Pedicle Screw System | NKB | 2022-08-09 | Ver |
| 510(k) | K220973 | CoreLink Navigation Instruments | OLO | 2022-06-01 | Ver |
| 510(k) | K211417 | F3D-C2 Cervical Stand-Alone System | OVE | 2022-02-04 | Ver |
| 510(k) | K214059 | CoreLink Navigation Instruments | OLO | 2022-01-19 | Ver |
| 510(k) | K212825 | CoreLink Navigation Instruments | OLO | 2021-10-13 | Ver |
| 510(k) | K210539 | CoreLink Midline Fixation System | NKB | 2021-04-15 | Ver |
| 510(k) | K202637 | F3D Corpectomy System | MQP | 2020-12-23 | Ver |
| 510(k) | K200087 | F3D Cervical Stand-Alone Interbody Fusion System | OVE | 2020-06-15 | Ver |
| 510(k) | K200863 | Tiger® Occipital-Cervical-Thoracic Spinal Fixation System | NKG | 2020-04-28 | Ver |
| 510(k) | K182731 | Corelink Navigation Instruments | OLO | 2019-12-13 | Ver |
| 510(k) | K190016 | Lateral Plate System | KWQ | 2019-06-12 | Ver |
| 510(k) | K183239 | CoreLink F3D™ Lateral System | MAX | 2018-12-19 | Ver |
| 510(k) | K180814 | CoreLink® M3™ Stand-Alone Anterior Lumbar System | OVD | 2018-08-10 | Ver |
| 510(k) | K180556 | Corelink Foundation 3D Anterior Lumbar System | MAX | 2018-07-27 | Ver |
No hay dispositivos coincidentes.