OSTEOFIL ICM MOLDABLE STRIP 002390

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2005-10-06 for OSTEOFIL ICM MOLDABLE STRIP 002390 manufactured by Regeneration Technologies, Inc..

Event Text Entries

[412409] Cervical c6-7 open reduction with fusion instrumentation. Osteofil 90 mm strip implanted. Infection diagnosed 2005.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002719998-2005-00011
MDR Report Key640225
Report Source08
Date Received2005-10-06
Date of Report2005-10-05
Date of Event2005-09-01
Date Mfgr Received2005-09-15
Device Manufacturer Date2004-03-01
Date Added to Maude2005-10-13
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 Location0
Manufacturer ContactAUDRA MCCONNELL
Manufacturer Street11621 RESEARCH CIRCLE P.O. BOX 2650
Manufacturer CityALACHUA FL 32616
Manufacturer CountryUS
Manufacturer Postal32616
Manufacturer Phone3864188888
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOSTEOFIL ICM MOLDABLE STRIP
Generic NameALLOGRAFT BONE PASTE
Product CodeLMO
Date Received2005-10-06
Model Number002390
Catalog Number002390
Lot Number101031946
ID NumberNA
Device Expiration Date2009-03-08
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Implant FlagY
Date Removed*
Device Sequence No1
Device Event Key629733
ManufacturerREGENERATION TECHNOLOGIES, INC.
Manufacturer Address* ALACHUA FL * US
Baseline Brand NameOSTEOFIL ICM MOLDABLE STRIP
Baseline Generic NameALLOGRAFT BONE PASTE
Baseline Model No002390
Baseline Catalog No002390
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-10-06

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