MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2017-09-13 for JOURNEY PFJ IMPLANT X-SM RT 71461011 manufactured by Smith & Nephew, Inc..
[86069323]
Patient Sequence No: 1, Text Type: N, H10
[86069324]
It was reported that a right knee journey pfj was revised to a tka due to progression of disease. The patella was inspected and left in situ.
Patient Sequence No: 1, Text Type: D, B5
[107872844]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1020279-2017-00743 |
| MDR Report Key | 6863319 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2017-09-13 |
| Date of Report | 2017-12-04 |
| Date of Event | 2017-08-23 |
| Date Mfgr Received | 2017-08-23 |
| Device Manufacturer Date | 2007-04-24 |
| Date Added to Maude | 2017-09-13 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MARKUS POETTKER |
| Manufacturer Street | 1450 BROOKS ROAD |
| Manufacturer City | MEMPHIS TN 38116 |
| Manufacturer Country | US |
| Manufacturer Postal | 38116 |
| Manufacturer G1 | SMITH & NEPHEW, INC. |
| Manufacturer Street | 1450 BROOKS ROAD |
| Manufacturer City | MEMPHIS TN 38116 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 38116 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | JOURNEY PFJ IMPLANT X-SM RT |
| Generic Name | PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
| Product Code | KRR |
| Date Received | 2017-09-13 |
| Catalog Number | 71461011 |
| Lot Number | 07DM17667 |
| Device Expiration Date | 2017-04-21 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SMITH & NEPHEW, INC. |
| Manufacturer Address | 1450 BROOKS ROAD MEMPHIS TN 38116 US 38116 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2017-09-13 |