FDA-Device2018-03-21Class II
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Argo Medical Technologies Ltd
Hazard
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Sold states
US and foreign.
Affected count
127
Manufactured in
Matambuilding 30p.O.Box 15054, Haifahaifa, Israel
Products
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0944-2018Don't want to check this manually?
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