ORTHOPEDIATRICS 3.2MM CANNULATED DRILL, SHORT N/A 01-1400-0017

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2020-03-11 for ORTHOPEDIATRICS 3.2MM CANNULATED DRILL, SHORT N/A 01-1400-0017 manufactured by Orthopediatrics, Inc.

MAUDE Entry Details

Report Number3006460162-2020-00043
MDR Report Key9820538
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2020-03-11
Date of Report2020-03-11
Date of Event2020-02-11
Date Mfgr Received2020-02-11
Device Manufacturer Date2018-08-01
Date Added to Maude2020-03-11
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 ContactKRISS ANDERSON
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW, IN
Manufacturer CountryUS
Manufacturer Phone2670872
Manufacturer G1ORTHOPEDIATRICS, INC
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW, IN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameORTHOPEDIATRICS 3.2MM CANNULATED DRILL, SHORT
Generic NameBIT, SURGICAL
Product CodeGFG
Date Received2020-03-11
Returned To Mfg2020-02-20
Model NumberN/A
Catalog Number01-1400-0017
Lot Number91902437-C
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerORTHOPEDIATRICS, INC
Manufacturer Address2850 FRONTIER DRIVE WARSAW, IN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.