SONIK MONARK 100— 510(k) K234036
Substantially EquivalentNeuro Spinal Innovation, Inc.
FDA 510(k) clearance K234036 for SONIK MONARK 100, Substantially Equivalent on 2024-02-15. Applicant: Neuro Spinal Innovation, Inc..
Clearance details
- Applicant
- Neuro Spinal Innovation, Inc.
- Product code
- Code LXM
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mississauga, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.