FDA Adverse Event
Injury
Summary report: N
HINTERMANN SERIES H3
MDR report key: 19166271
·
Received April 23, 2024
Report
- Report Number
- 3012104767-2024-00000
- Event Type
- Injury
- Date Received
- April 23, 2024
- Date of Event
- March 27, 2024
- Report Date
- April 22, 2024
- Manufacturer
- DT MEDTECH LLC, A VILEX COMPANY
- Product Code
- NTG
- PMA / PMN Number
- P160036
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- 003
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HINTERMANN SERIES H3 | TOTAL ANKLE REPLACEMENT | NTG | DT MEDTECH LLC, A VILEX COMPANY | 300205 | AABII |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |