Regulatory filing

K241822 (us_fda)

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

fda 510k · cleared · decided 2024-12-01

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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

Covered models (1)

ReWalk 7

Sources (1)

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241822

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Identity

43414cae-17d5-45d1-a217-3c34f1dd001a