MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1999-05-20 for TMJ FOSSA-EMINENCE & TMJ CONDYLAR PROSTHESIS SYSTEM CS-027-08/10 manufactured by Tmj Implants, Inc..
[156843]
Surgeon states loose screws and pain.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1721760-1999-00019 |
| MDR Report Key | 224360 |
| Report Source | 05 |
| Date Received | 1999-05-20 |
| Date of Report | 1999-04-23 |
| Date of Event | 1999-03-16 |
| Report Date | 1999-04-23 |
| Date Reported to Mfgr | 1999-04-23 |
| Date Mfgr Received | 1999-04-23 |
| Date Added to Maude | 1999-05-25 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TMJ FOSSA-EMINENCE & TMJ CONDYLAR PROSTHESIS SYSTEM |
| Generic Name | CONDYLAR SCREWS |
| Product Code | MPL |
| Date Received | 1999-05-20 |
| Model Number | NA |
| Catalog Number | CS-027-08/10 |
| Lot Number | (2990) (5555) & (6035) |
| ID Number | NA |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | Y |
| Date Removed | V |
| Device Sequence No | 1 |
| Device Event Key | 217564 |
| Manufacturer | TMJ IMPLANTS, INC. |
| Manufacturer Address | 17301 WEST COLFAX AVE. #135 GOLDEN CO 80401 US |
| Baseline Brand Name | TMK FOSSA-EMINENCE & TMJ CONDYLAR PROSTHESIS SYSTEM |
| Baseline Generic Name | CONDYLAR SCREWS |
| Baseline Model No | NA |
| Baseline Catalog No | CS-027-08/10 |
| Baseline ID | NA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 1999-05-20 |