MAXFRAME(TM) QUICK ADJUST STRUT/MEDIUM 03.312.812

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-19 for MAXFRAME(TM) QUICK ADJUST STRUT/MEDIUM 03.312.812 manufactured by Wrights Lane Synthes Usa Products Llc.

Event Text Entries

[188665838] Product complaint # (b)(4). Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received. The investigation could not be completed; no conclusion could be drawn at the time of filing this report. A review of the device history record has been requested. Device was used for treatment, not diagnosis. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[188665839] It was reported that on an unknown date, during a routine incoming inspection of a loaner set, it was observed that a maxframe strut with quick adjust was broken there was no known patient or hospital involvement. This complaint involves one (1) device. This report is 2 of 2 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2939274-2020-01388
MDR Report Key9857727
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-19
Date of Report2020-02-21
Date Mfgr Received2020-02-21
Date Added to Maude2020-03-19
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 ContactKARA DITTY-BOVARD
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone6103142063
Manufacturer G1MONUMENT
Manufacturer Street1101 SYNTHES AVENUE
Manufacturer CityMONUMENT CO
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAXFRAME(TM) QUICK ADJUST STRUT/MEDIUM
Generic NameAPPLIANCE,FIXATION,NAIL
Product CodeKTT
Date Received2020-03-19
Model Number03.312.812
Catalog Number03.312.812
Lot Number14L6187
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerWRIGHTS LANE SYNTHES USA PRODUCTS LLC
Manufacturer Address1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 US 19380


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-19

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