ARCS ANCHORS * UNK BONE A

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number1221934-2004-00083
MDR Report Key530791
Report Source00,07
Date Received2004-06-22
Date of Report2004-06-17
Report Date2004-06-17
Date Mfgr Received2004-06-17
Date Added to Maude2004-06-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. RONALD GIANNANGELO
Manufacturer Street60 GLACIER DRIVE
Manufacturer CityWESTWOOD MA 02090
Manufacturer CountryUS
Manufacturer Postal02090
Manufacturer Phone7812513195
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameARCS ANCHORS
Generic NameBONE ANCHOR
Product CodeNOV
Date Received2004-06-22
Model Number*
Catalog NumberUNK BONE A
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedU
Device Sequence No1
Device Event Key520029
ManufacturerDEPUY MITEK
Manufacturer Address60 GLACIER DRIVE WESTWOOD MA 02090 US
Baseline Brand NameARCS ANCHORS
Baseline Generic NameBONE ANCHOR
Baseline Model NoUNK
Baseline Catalog NoUNK BONE A
Baseline IDUNK


Patients

Patient NumberTreatmentOutcomeDate
10 2004-06-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.