RT Elements (4.5); (Elements) Multiple Brain Mets SRS; (Elements) Cranial SRS; (Elements) Spine SRS; (Elements) Cranial SRS w/ Cones; (Elements) RT Planning Platform; (Elements) Dose Review; (Elements) Retreatment Review; Elements Segmentation [Cranial , Basal Ganglia, Head & Neck, Pelvic, Spine, Thoracic & Spine, Extracranial] RT; Elements AI Tumor Segmentation RT; Elements SmartBrush [Angio, Spine] RT; Elements Object Management RT
K250440 is the FDA 510(k) clearance record for RT Elements (4.5); (Elements) Multiple Brain Mets SRS; (Elements) Cranial SRS; (Elements) Spine SRS; (Elements) Cranial SRS w/ Cones; (Elements) RT Planning Platform; (Elements) Dose Review; (Elements) Retreatment Review; Elements Segmentation [Cranial , Basal Ganglia, Head & Neck, Pelvic, Spine, Thoracic & Spine, Extracranial] RT; Elements AI Tumor Segmentation RT; Elements SmartBrush [Angio, Spine] RT; Elements Object Management RT, a class II device, cleared for Brainlab AG on under FDA product code MUJ (System, Planning, Radiation Therapy Treatment). FDA records list 146 510(k) clearances for Brainlab AG, from to . As of , FDA records show no recalls naming K250440.
Clearance record
- Decision date
- Received
- (123 days to decision)
- Product code
- MUJ System, Planning, Radiation Therapy Treatment
- Regulation
- 21 CFR 892.5050
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Brainlab AG Olof-Palme-Str 9, Munich, DE
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MUJ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 3 |
| January 2026 | 0 |
| February 2026 | 2 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 3 |
| June 2026 | 1 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
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