FDA Adverse Event
Injury
Summary report: N
REWALK PERSONAL 5.0
MDR report key: 6224003
·
Received January 4, 2017
Report
- Report Number
- 3007615665-2017-00001
- Event Type
- Injury
- Date Received
- January 4, 2017
- Date of Event
- November 21, 2016
- Report Date
- January 4, 2017
- Manufacturer
- REWALK ROBOTICS LTD.
- Product Code
- PHL
- PMA / PMN Number
- K131798
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
HAD A CALCANEAL FRACTURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 3880 | REWALK PERSONAL 5.0 | POWERED EXOSKELETON | PHL | REWALK ROBOTICS LTD. | PERSONAL |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |