5.5/6.0 UNIAXIAL PEDICLE SCREW 6.0MM, 45MM N/A 00-1300-0645

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 2019-06-05 for 5.5/6.0 UNIAXIAL PEDICLE SCREW 6.0MM, 45MM N/A 00-1300-0645 manufactured by Orthopediatrics, Inc.

MAUDE Entry Details

Report Number3006460162-2019-00021
MDR Report Key8671958
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-06-05
Date of Report2019-06-05
Date of Event2019-05-03
Date Mfgr Received2019-05-06
Date Added to Maude2019-06-05
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 ContactLEIGH JESSOP
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745490872
Manufacturer G1ORTHOPEDIATRICS, INC
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name5.5/6.0 UNIAXIAL PEDICLE SCREW 6.0MM, 45MM
Generic NamePEDICLE SCREW SPINAL SYSTEM, ADOLESCENT IDIOPATHIC SCOLIOSIS
Product CodeOSH
Date Received2019-06-05
Model NumberN/A
Catalog Number00-1300-0645
Lot Number045888-G
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerORTHOPEDIATRICS, INC
Manufacturer Address2850 FRONTIER DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-05

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