MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2007-01-02 for PRSVN MB INSERT SZ3 11.5MM 149815310 manufactured by Depuy Orthopaedics, Depuy-cork.
[589163]
Patient was revised to address pain in the knee.
Patient Sequence No: 1, Text Type: D, B5
[7914103]
This complaint is still under investigation. Depuy will notify the fda of the results of this investigation once it has been completed.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1818910-2006-04336 |
MDR Report Key | 801160 |
Report Source | 05,08 |
Date Received | 2007-01-02 |
Date of Report | 2006-12-12 |
Date of Event | 2006-12-12 |
Date Mfgr Received | 2006-12-12 |
Date Added to Maude | 2007-01-09 |
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 | 0 |
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 ORTHOPAEDICS |
Manufacturer Street | LOUGHBEG |
Manufacturer City | RINGASKIDDY CTY, CORK |
Manufacturer Country | EI |
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 INSERT SZ3 11.5MM |
Generic Name | 87MBD |
Product Code | MBD |
Date Received | 2007-01-02 |
Model Number | NA |
Catalog Number | 149815310 |
Lot Number | 1044192 |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | Y |
Date Removed | V |
Device Sequence No | 1 |
Device Event Key | 788700 |
Manufacturer | DEPUY ORTHOPAEDICS, DEPUY-CORK |
Manufacturer Address | LOUGHBEG RINGASKIDDY CTY, CORK EI |
Baseline Brand Name | PRSVN MB INSERT SZ3 11.5MM |
Baseline Generic Name | KNEE INSERT |
Baseline Model No | NA |
Baseline Catalog No | 149815310 |
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 | 2007-01-02 |