Medos International SARL
FDA 510(k) & PMA Approved Dispositivos — 75 products
Publicidad
Total de dispositivos75
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K254157 | CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody | OLO | 2026-05-26 | Ver |
| 510(k) | K260240 | SYMPHONY Navigation Ready Instruments | OLO | 2026-03-27 | Ver |
| 510(k) | K253249 | TriALTIS™ Spine System | NKB | 2025-10-21 | Ver |
| 510(k) | K243249 | TriALTIS™ Spine System | NKB | 2025-01-17 | Ver |
| 510(k) | K241893 | CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays | OLO | 2024-09-16 | Ver |
| 510(k) | K242042 | TriALTIS™ Spine System | NKB | 2024-09-09 | Ver |
| 510(k) | K233684 | TriALTIS™ Spine System | NKB | 2023-12-12 | Ver |
| 510(k) | K233366 | SYMPHONY OCT System | NKG | 2023-11-09 | Ver |
| 510(k) | K232492 | 2.7 mm GRYPHON™ Flex Knotless PEEK Anchor; 2.7 mm GRYPHON™ Flex Knotless Biocomposite Anchor | MBI | 2023-10-06 | Ver |
| 510(k) | K231479 | TriALTIS Spine System | NKB | 2023-09-22 | Ver |
| 510(k) | K223438 | TELIGEN System Peripheral Motor Nerve Stimulation Indications | PDQ | 2023-02-10 | Ver |
| 510(k) | K223108 | TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) | OLO | 2023-01-19 | Ver |
| 510(k) | K213978 | TELIGEN System | HRX | 2022-10-18 | Ver |
| 510(k) | K222473 | EXPEDIUM® Spine System, EXPEDIUM VERSE® Spine System: ALTALYNE™ Ultra Rods | NKB | 2022-10-13 | Ver |
| 510(k) | K221325 | CONDUIT Lateral Switch Plate | MAX | 2022-08-25 | Ver |
| 510(k) | K220040 | CEREPAK Uniform, Uniform XL, Uniform 3D, Heliform Soft, Heliform XtraSoft, Heliform XL, Heliform XtraSoft XL, Freeform, Freeform Mini, and Freeform XtraSoft Detachable Coil Systems | HCG | 2022-07-14 | Ver |
| 510(k) | K221364 | Mitek TIGHT-N Anchor | MBI | 2022-07-11 | Ver |
| 510(k) | K212756 | Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set | OLO | 2022-05-05 | Ver |
| 510(k) | K220219 | PERMALOOP Suture, PERMATAPE Suture | GAT | 2022-04-26 | Ver |
| 510(k) | K214025 | PROWLER SELECT LP ES Microcatheter; PROWLER XS Microcatheter | KRA | 2022-04-12 | Ver |
No hay dispositivos coincidentes.