MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2005-05-24 for PRSVN MB TIB TRAY RM/LL CEM S2 149825002 manufactured by Depuy International, Ltd..
[388702]
Bilateral was revised due to loosening of the tibial components.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2005-00762 |
MDR Report Key | 604776 |
Report Source | 05,08 |
Date Received | 2005-05-24 |
Date of Report | 2005-05-19 |
Date of Event | 2005-05-19 |
Date Facility Aware | 2005-05-19 |
Report Date | 2005-05-19 |
Date Mfgr Received | 2005-05-19 |
Device Manufacturer Date | 2003-04-01 |
Date Added to Maude | 2005-05-25 |
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 | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | GINNY STAMBERGER, MGR. |
Manufacturer Street | 700 ORTHOPAEDIC DRIVE |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 5743727333 |
Manufacturer G1 | DEPUY INTERNATIONAL, LTD. |
Manufacturer Street | ST. ANTHONY'S ROAD |
Manufacturer City | LEEDS, |
Manufacturer Country | UK |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PRSVN MB TIB TRAY RM/LL CEM S2 |
Generic Name | TOTAL KNEE REPLACEMENT |
Product Code | MBD |
Date Received | 2005-05-24 |
Model Number | NA |
Catalog Number | 149825002 |
Lot Number | YML60 |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 1 YR |
Device Eval'ed by Mfgr | R |
Implant Flag | Y |
Date Removed | V |
Device Sequence No | 1 |
Device Event Key | 594563 |
Manufacturer | DEPUY INTERNATIONAL, LTD. |
Manufacturer Address | ST. ANTHONY'S ROAD LEEDS UK LS11 8DT |
Baseline Brand Name | PRSVN MB TIB TRAY RM/LL CEM S2 |
Baseline Generic Name | KNEE INSERT |
Baseline Model No | NA |
Baseline Catalog No | 149825002 |
Baseline ID | NA |
Baseline Device Family | PRSVN MB INSERT |
Baseline Shelf Life Contained | N |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | Y |
Premarket Approval | P9100 |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2005-05-24 |