510(k) K241822 · PHL Powered Exoskeleton
ReWalk® 7 Personal Exoskeleton (50-20-0005)
| Applicant | Rewalk Robotics Ltd. Dba Lifeward, Yokneam Ilit, IL |
| Decision | Substantially Equivalent, Mar 12, 2025 |
| Received | Jun 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241822
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.