MEDPOR CUSTOMIZED CRANIAL-L 54440310

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-11-26 for MEDPOR CUSTOMIZED CRANIAL-L 54440310 manufactured by Stryker Orthobiologics-malvern.

MAUDE Entry Details

Report Number0008010177-2019-00074
MDR Report Key9375806
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-11-26
Date of Report2019-11-26
Date of Event2019-11-08
Date Mfgr Received2019-11-08
Date Added to Maude2019-11-26
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. KELLI DYKSTRA
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer PostalD-79111
Manufacturer Phone76145120
Manufacturer G1STRYKER ORTHOBIOLOGICS-MALVERN
Manufacturer Street45 GREAT VALLEY PARKWAY
Manufacturer CityMALVERN PA 19355
Manufacturer CountryUS
Manufacturer Postal Code19355
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEDPOR CUSTOMIZED CRANIAL-L
Generic NameIMPLANT
Product CodeFWP
Date Received2019-11-26
Catalog Number54440310
Lot Number1906241020
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ORTHOBIOLOGICS-MALVERN
Manufacturer Address45 GREAT VALLEY PARKWAY MALVERN PA 19355 US 19355


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-26

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