FDA Adverse Event
Other
Summary report: N
UNI-KNEE TIBIA INSERT 9MM SIZE 3.4
MDR report key: 56442
·
Received December 18, 1996
Report
- Report Number
- 2935620-1996-00015
- Event Type
- Other
- Date Received
- December 18, 1996
- Date of Event
- November 13, 1996
- Report Date
- December 17, 1996
- Manufacturer
- INTERMEDICS ORTHOPEDICS, INC.
- Product Code
- HRY
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
NOTIFICATION OF DELAY IN SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNI-KNEE TIBIA INSERT 9MM SIZE 3.4 Implant | KNEE IMPLANT PROSTHESIS | HRY | INTERMEDICS ORTHOPEDICS, INC. | NA | 1232502 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Other | 6100-00-130 |