UNKNOWN_FRO_PRODUCT UNK_FRO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-03-28 for UNKNOWN_FRO_PRODUCT UNK_FRO manufactured by Stryker Leibinger Freiburg.

Event Text Entries

[41310572] Device is not available for evaluation. If additional information is received, it will be reported on a supplemental report. Device remains implanted.
Patient Sequence No: 1, Text Type: N, H10


[41310573] A company representative reported a complaint for a medpor custom cranial implant. In this complaint, a patient has developed an infection after implantation. No other information is known at this time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0008010177-2016-00056
MDR Report Key5530291
Date Received2016-03-28
Date of Report2016-03-08
Date of Event2016-03-07
Date Mfgr Received2016-03-08
Date Added to Maude2016-03-28
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. JONATHAN SCHELL
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 NameUNKNOWN_FRO_PRODUCT
Generic NameIMPLANT
Product CodeFWP
Date Received2016-03-28
Catalog NumberUNK_FRO
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER LEIBINGER FREIBURG
Manufacturer AddressBOETZINGERSTR. 41 FREIBURG D-79111 D-79111


Patients

Patient NumberTreatmentOutcomeDate
10 2016-03-28

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