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 2017-12-07 for CENTERPIECE PLATE FIXATION SYSTEM G9010000274 manufactured by Warsaw Orthopedics.

Event Text Entries

[94251061] This product is not approved for sale in us but a similar device with catalog# 853-465,510k # k050082 and udi (b)(4) is approved for sale in us. Neither the device nor applicable imaging films were returned to manufacturer for evaluation therefore we are unable to determine the definitive cause of event.
Patient Sequence No: 1, Text Type: N, H10


[94251062] It was reported that on an unknown date the patient underwent laminoplasty due to cervical spondylotic myelopathy. Allegedly post-op, the screw in the lamina side backed out. The screw still remains in the patient. As there were no symptoms in particular, revision surgery was not scheduled.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1030489-2017-02466
MDR Report Key7094726
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2017-12-07
Date of Report2017-12-07
Date of Event2017-11-09
Date Mfgr Received2017-11-09
Date Added to Maude2017-12-07
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 Received2017-12-07
Model NumberNA
Catalog NumberG9010000274
Lot NumberUNK
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
10 2017-12-07

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