FDA Adverse Event
Injury
Summary report: N
TMJ IMPLANT
MDR report key: 26295
·
Received September 29, 1995
Report
- Report Number
- MW1007151
- Event Type
- Injury
- Date Received
- September 29, 1995
- Date of Event
- February 1, 1994
- Manufacturer
- OSTEOMED CORP.
- Product Code
- LZD
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
TMJ IMPLANT BROKE AFTER LESS THAN 1 YRS USE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TMJ IMPLANT Implant | TMJ IMPLANT | LZD | OSTEOMED CORP. | MAXI M-3 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 40 YR | Hospitalization| R| S |