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 |