K260142
- 510(k) number
- K260142
- Device name
- StimelMD (SSMD) system
- Applicant
- Motion Informatics ltd. IL
- Product code
- IPF — Stimulator, Muscle, Powered
- Decision date
- 2026-05-27
- Date received
- 2026-01-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K260142.pdf
Official FDA record: K260142
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.