K234036
- 510(k) number
- K234036
- Device name
- SONIK MONARK 100
- Applicant
- Neuro Spinal Innovation, Inc. CA
- Product code
- LXM — Manipulator, Plunger-Like Joint
- Decision date
- 2024-02-15
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K234036.pdf
Official FDA record: K234036
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.