CD HORIZON SPINAL SYSTEM 8115558

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 2020-03-22 for CD HORIZON SPINAL SYSTEM 8115558 manufactured by Warsaw Orthopedics.

Event Text Entries

[184442494] Product was not 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


[184442495] It was reported that the patient presented with lumbar degeneration; and underwent posterior lumbar decompression and fusion. Intra-op, the alleged implant broke. The broken implant was then completely explanted with no broken fragments remaining inside the patient. The broken product was replaced with a new one, and the surgery was completed. No patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1030489-2020-00352
MDR Report Key9863799
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-22
Date of Report2020-03-22
Date of Event2020-02-24
Date Mfgr Received2020-02-25
Device Manufacturer Date2017-07-26
Date Added to Maude2020-03-22
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 NameCD HORIZON SPINAL SYSTEM
Generic NameAPPLIANCE, FIXATION, SPINAL INTERLAMINAL
Product CodeKWP
Date Received2020-03-22
Model NumberNA
Catalog Number8115558
Lot Number0581899W
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 2020-03-22

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