MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,07 report with the FDA on 2004-06-22 for ARCS ANCHORS * UNK BONE A manufactured by Depuy Mitek.
[336897]
A statement was made to a depuy mitek employee that there was a pt infection involving a depuy mitek product.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1221934-2004-00083 |
MDR Report Key | 530791 |
Report Source | 00,07 |
Date Received | 2004-06-22 |
Date of Report | 2004-06-17 |
Report Date | 2004-06-17 |
Date Mfgr Received | 2004-06-17 |
Date Added to Maude | 2004-06-23 |
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 | MR. RONALD GIANNANGELO |
Manufacturer Street | 60 GLACIER DRIVE |
Manufacturer City | WESTWOOD MA 02090 |
Manufacturer Country | US |
Manufacturer Postal | 02090 |
Manufacturer Phone | 7812513195 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARCS ANCHORS |
Generic Name | BONE ANCHOR |
Product Code | NOV |
Date Received | 2004-06-22 |
Model Number | * |
Catalog Number | UNK BONE A |
Lot Number | UNK |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | Y |
Date Removed | U |
Device Sequence No | 1 |
Device Event Key | 520029 |
Manufacturer | DEPUY MITEK |
Manufacturer Address | 60 GLACIER DRIVE WESTWOOD MA 02090 US |
Baseline Brand Name | ARCS ANCHORS |
Baseline Generic Name | BONE ANCHOR |
Baseline Model No | UNK |
Baseline Catalog No | UNK BONE A |
Baseline ID | UNK |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2004-06-22 |