UNKNOWN PERFORATOR PSS UNKNOWN

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 2019-09-17 for UNKNOWN PERFORATOR PSS UNKNOWN manufactured by Mdt Powered Surgical Solutions.

MAUDE Entry Details

Report Number1625507-2019-00098
MDR Report Key9079626
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-09-17
Date of Report2019-10-10
Date of Event2019-08-01
Date Mfgr Received2019-09-12
Date Added to Maude2019-09-17
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 ContactTRICHA MILES
Manufacturer Street4620 NORTH BEACH STREET
Manufacturer CityFT. WORTH TX 761373291
Manufacturer CountryUS
Manufacturer Postal761373291
Manufacturer Phone9496801224
Manufacturer G1MDT POWERED SURGICAL SOLUTIONS
Manufacturer Street4620 N BEACH ST
Manufacturer CityFORT WORTH TX 76137
Manufacturer CountryUS
Manufacturer Postal Code76137
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN PERFORATOR
Generic NameDRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOUND, POWERED)
Product CodeHBF
Date Received2019-09-17
Model NumberPSS UNKNOWN
Catalog NumberPSS UNKNOWN
Lot NumberUNKNOWN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMDT POWERED SURGICAL SOLUTIONS
Manufacturer Address4620 N BEACH ST FORT WORTH TX 76137 US 76137


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2019-09-17

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