ESCALATE EXPANDABLE PLATE 48570300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-06 for ESCALATE EXPANDABLE PLATE 48570300 manufactured by Stryker Spine-us.

Event Text Entries

[99223233] It was reported that during a procedure, a plate was over expanded and came apart. The plate was taken out and replaced. There was a reported delay of 4/5 minutes. The procedure was completed successfully and there are no reports of adverse consequences.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009617544-2018-00034
MDR Report Key7244905
Date Received2018-02-06
Date of Report2018-05-24
Date of Event2018-01-11
Date Mfgr Received2018-04-26
Device Manufacturer Date2017-02-24
Date Added to Maude2018-02-06
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. MARTA KOUTSOGIANNIS
Manufacturer Street2 PEARL COURT
Manufacturer CityALLENDALE NJ 07401
Manufacturer CountryUS
Manufacturer Postal07401
Manufacturer Phone2017608000
Manufacturer G1STRYKER SPINE-FRANCE
Manufacturer StreetZONE INDUSTRIELLE DE MARTICOT
Manufacturer CityCESTAS 33610
Manufacturer CountryFR
Manufacturer Postal Code33610
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameESCALATE EXPANDABLE PLATE
Generic NameSPINAL INTERLAMINAL FIXATION ORTHOSI
Product CodeNQW
Date Received2018-02-06
Returned To Mfg2018-01-29
Model Number48570300
Catalog Number48570300
Lot Number16A617
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER SPINE-US
Manufacturer Address2 PEARL COURT ALLENDALE NJ 07401 US 07401


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-06

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