# K241822 (us_fda)

FDA 510(k) K241822 for ReWalk 7 Personal Exoskeleton. Newest generation personal exoskeleton for home use.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K241822
- Filing date: 2024-06-24
- Decision date: 2024-12-01
- Verification posture: verified

## Applicant

- [Lifeward](/companies/lifeward.md)

## Covered models (1)

- [ReWalk 7](/models/rewalk-7.md)

## Sources (1)

- [https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241822](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241822)

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