FDA Adverse Event
Malfunction
Summary report: N
TI TITAMAX IMPLANT (5.0) 5.0X7
MDR report key: 5014260
·
Received August 5, 2015
Report
- Report Number
- 3010593814-2015-01474
- Event Type
- Malfunction
- Date Received
- August 5, 2015
- Date of Event
- January 1, 2015
- Report Date
- May 4, 2015
- Manufacturer
- NEODENT
- Product Code
- DZE
- PMA / PMN Number
- K101207
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- BR
- Reporter Occupation
- DENTIST
Narratives
Additional Manufacturer Narrative · 1
(B)(4). INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF (B)(4).
Description of Event or Problem · 1
(B)(4). THE DENTIST REPORTED THAT 42 DAYS AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION #31 IT WAS VERIFIED ITS NON OSSEOINTEGRATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 519095 | TI TITAMAX IMPLANT (5.0) 5.0X7 | ENDOSSEOUS DENTAL IMPLANT | DZE | NEODENT | NA | 800099568 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |