CORMATRIX ECM FOR VASCULAR REPAIR CMCV-014-609

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-08-19 for CORMATRIX ECM FOR VASCULAR REPAIR CMCV-014-609 manufactured by Aziyo Biologics, Inc..

MAUDE Entry Details

Report Number3005619880-2019-00009
MDR Report Key8908117
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-08-19
Date of Report2019-08-19
Date of Event2019-07-01
Date Mfgr Received2019-07-23
Device Manufacturer Date2015-04-24
Date Added to Maude2019-08-19
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. ANDREW GREEN
Manufacturer Street1100 OLD ELLIS ROAD STE 1200
Manufacturer CityROSWELL GA 30076
Manufacturer CountryUS
Manufacturer Postal30076
Manufacturer G1AZIYO BIOLOGICS, INC.
Manufacturer Street1100 OLD ELLIS ROAD STE 1200
Manufacturer CityROSWELL GA 30076
Manufacturer CountryUS
Manufacturer Postal Code30076
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCORMATRIX ECM FOR VASCULAR REPAIR
Generic NamePATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
Product CodeDXZ
Date Received2019-08-19
Model NumberCMCV-014-609
Lot NumberM15D1104
Device Expiration Date2016-07-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAZIYO BIOLOGICS, INC.
Manufacturer Address1100 OLD ELLIS ROAD STE 1200 ROSWELL GA 30076 US 30076


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening; 2. Required No Informationntervention 2019-08-19

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