CENTERPIECE PLATE FIXATION SYSTEM G9010000274

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-05-22 for CENTERPIECE PLATE FIXATION SYSTEM G9010000274 manufactured by Warsaw Orthopedics.

Event Text Entries

[145742694] This part is not approved for use in the united states; however a like device catalog#853-507, 510k#k050082, udi# (b)(4)?? Was cleared in the united states. H6: neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[145742695] It was reported that the patient underwent laminoplasty due to cervical spondylotic myelopathy (csm). Post-op, the lateral mass screw of the centerpiece migrated and entered into the spinal canal. Patient suffered with palsy occurred at c5 as a result of this event. There is not plan for revision surgery yet.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1030489-2019-00573
MDR Report Key8631202
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-05-22
Date of Report2019-05-22
Date of Event2019-04-17
Date Mfgr Received2019-05-07
Date Added to Maude2019-05-22
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 ContactSTACIE ZIEMBA
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal38132
Manufacturer Phone9013963133
Manufacturer G1WARSAW ORTHOPEDICS
Manufacturer Street2500 SILVEUS CROSSING
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCENTERPIECE PLATE FIXATION SYSTEM
Generic NameORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL
Product CodeNQW
Date Received2019-05-22
Model NumberNA
Catalog NumberG9010000274
Lot Number0678228W
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerWARSAW ORTHOPEDICS
Manufacturer Address2500 SILVEUS CROSSING WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-05-22

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