MEDPOR CUSTOMIZED CRANIAL-XL 54440410

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-07-12 for MEDPOR CUSTOMIZED CRANIAL-XL 54440410 manufactured by Stryker Orthobiologics-malvern.

Event Text Entries

[49371247] Device is not available for evaluation. If additional information is received it will be reported on a supplemental report. Device still implanted in patient.
Patient Sequence No: 1, Text Type: N, H10


[49371248] It was reported that the original surgery for this patient took place in (b)(6) 2015. A revision surgery needs to be rescheduled, as the patient has acquired an infection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2016-00148
MDR Report Key5788019
Date Received2016-07-12
Date of Report2016-06-21
Date of Event2016-06-21
Date Mfgr Received2016-06-21
Date Added to Maude2016-07-12
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 Report0

Device Details

Brand NameMEDPOR CUSTOMIZED CRANIAL-XL
Generic NameIMPLANT
Product CodeFWP
Date Received2016-07-12
Catalog Number54440410
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. Other 2016-07-12

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