SPF PLUS-MINI (60 ?A/M) N/A 10-1398M

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-06-17 for SPF PLUS-MINI (60 ?A/M) N/A 10-1398M manufactured by Ebi, Llc..

MAUDE Entry Details

Report Number0002242816-2019-00018
MDR Report Key8705747
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-06-17
Date of Report2019-07-05
Date of Event2019-05-30
Date Mfgr Received2019-07-03
Device Manufacturer Date2019-01-24
Date Added to Maude2019-06-17
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 ContactSHAAN POLIUS
Manufacturer Street399 JEFFERSON ROAD
Manufacturer CityPARSIPPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal07054
Manufacturer Phone9732999300
Manufacturer G1EBI, LLC.
Manufacturer Street399 JEFFERSON ROAD
Manufacturer CityPARSIPPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal Code07054
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameSPF PLUS-MINI (60 ?A/M)
Generic NameSPF-PLUS 60/M, SPINAL FUSION STIMULATOR
Product CodeLOE
Date Received2019-06-17
Model NumberN/A
Catalog Number10-1398M
Lot NumberN/A
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerEBI, LLC.
Manufacturer Address399 JEFFERSON ROAD PARSIPPANY NJ 07054 US 07054


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-17

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