Brainlab SE
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262257 | Spine Planning (3.0); Spine & Trauma Navigation; Alignment System Spine | OLO | 2026-09-30 | View |
| 510(k) | K254010 | ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface | IYE | 2026-01-14 | View |
No matching devices.
Advertisement