STRATAFIX SXPD2B202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-07-10 for STRATAFIX SXPD2B202 manufactured by Surgical Specialties Corporation.

MAUDE Entry Details

Report Number3010692967-2019-00021
MDR Report Key8776040
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-07-10
Date of Report2019-07-10
Date of Event2019-06-16
Date Facility Aware2019-06-16
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2019-06-28
Date Mfgr Received2019-06-28
Date Added to Maude2019-07-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. RONALD GIANNANGELO
Manufacturer Street247 STATION DRIVE SUITE NE1
Manufacturer CityWESTWOOD MA 02090
Manufacturer CountryUS
Manufacturer Postal02090
Manufacturer G1SURGICAL SPECIALTIES CORPORATION
Manufacturer StreetRD 495 MONTANA INDUSRIAL PARK
Manufacturer CityAGUADILLA PR 00605
Manufacturer CountryUS
Manufacturer Postal Code00605
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTRATAFIX
Generic NameSTRAFIX PDO
Product CodeGAB
Date Received2019-07-10
Model NumberSXPD2B202
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSURGICAL SPECIALTIES CORPORATION
Manufacturer AddressRD. 495 MONTANA INDUSTRIAL PK AGUADILLA PR 00605 US 00605


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-10

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