K233006
- 510(k) number
- K233006
- Device name
- MyndMove, MyndMove 2.0
- Applicant
- Myndtec, Inc. CA
- Product code
- GZI — Stimulator, Neuromuscular, External Functional
- Decision date
- 2024-06-25
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233006.pdf
Official FDA record: K233006
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.