K251682
- 510(k) number
- K251682
- Device name
- MuscleView 2.0
- Applicant
- Springbok, Inc. (Dba Springbok Analytics) VA · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2025-09-09
- Date received
- 2025-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K251682.pdf
Official FDA record: K251682
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.