Regulatory filing

fda_510k (us_fda)

Wandercraft robotic exoskeleton wins expanded FDA clearance for spinal cord injury indication extension.

fda 510k · cleared · decided 2026-01-01

Track fda_510k (us_fda)

Machine-readable surfaces

Markdown mirror: /regulatory-filings/wandercraft-expanded-fda-nod.md
JSON-LD: embedded in this page’s head
REST API: /v1/filings/9a5d8e56-804b-435f-ba59-e75707da4714
Revision history: /regulatory-filings/wandercraft-expanded-fda-nod/history
Data documentation: /data
Query this programmatically: Deploy MCP

Key facts

Jurisdiction: us_fda
Filing type: fda 510k
Status: cleared
Decision date: 2026-01-01

Covered models (1)

Wandercraft Atalante X

Sources (1)

https://www.odtmag.com/breaking-news/wandercraft-robotic-exoskeleton-wins-expanded-fda-nod/

Deploy Watch

Track fda_510k (us_fda).

We notify you when the filing status changes or related filings, incidents, or litigations surface.

Identity

9a5d8e56-804b-435f-ba59-e75707da4714