K232077
- 510(k) number
- K232077
- Device name
- Atalante X
- Applicant
- Wandercraft SAS FR
- Product code
- PHL — Powered Exoskeleton
- Decision date
- 2023-12-13
- Date received
- 2023-07-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232077.pdf
Official FDA record: K232077
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.