IMPLANTIUM
Report
- Report Number
- 3005503242-2010-00099
- Event Type
- Injury
- Date Received
- December 9, 2010
- Date of Event
- September 22, 2010
- Report Date
- November 10, 2010
- Manufacturer
- DENTIUM USA
- Product Code
- DZE
- PMA / PMN Number
- K041368
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WA, US
- Reporter Occupation
- DENTIST
Narratives
CONCLUSION: BASED ON INSPECTION RESULTS AND THE DHR REVIEW, THE RETURNED PRODUCT HAS BEEN FOUND TO BE WITHIN SPECIFICATION. LACK OF OSSEOINTEGRATION IS A KNOWN ADVERSE EFFECT FOR ALL DENTAL IMPLANTS AS STATED IN OUR IFU. THE OVERALL SUCCESS RATE FOR DENTAL IMPLANTS IS ABOUT 95%. THEREFORE, THE IMPLANT FAILURE IS MOST LIKELY DUE TO CAUSES OTHER THAN THE PRODUCT SUCH AS SURGICAL MISTAKE, PT BONE CONDITION, PT ORAL HYGIENE, OR PT BEHAVIOR. ADDITIONALLY THE PT WAS REPORTED TO HAVE HYPERTENSION, WHICH IS A CHRONIC MEDICAL CONDITION IN WHICH THE SYSTEMIC ARTERIAL BLOOD PRESSURE IS ELEVATED.
BASED ON THE REPORT, THE PRODUCT WAS RETURNED AS AN IMPLANT FAILURE BECAUSE OF EARLY LOADING (POSSIBLE) AND PT HEALTH HABIT. PT HAS A REPORTED MEDICAL HISTORY OF HYPERTENSION. BASED ON THE REPORT, THE PT HAD MODERATE ORAL HYGIENE AND MODERATE BONE CONDITION. THE FIXTURE WAS PLACED WITH A TRADITIONAL TWO STAGE SURGERY WITH PRIMARY CLOSURE IN TOOTH LOCATION #10. XENOGRAPH BONE MATERIAL WAS USED. THE DOCTOR INDICATED THAT THE DEVICE WAS NOT RECEIVED DAMAGED OR DEFECTIVE SUCH THAT IT WOULD NOT PERFORM AS INTENDED. THE PT OUTCOME WAS REPORTED AS STABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | IMPLANTIUM | ENDOSSEOUS DENTAL IMPLANT | DZE | DENTIUM USA | FX3812MLC | B15XA110S |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 79 YR | Required Intervention |