HTR-PEKK PK620898

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-19 for HTR-PEKK PK620898 manufactured by Oxford Performance Materials.

Event Text Entries

[114536974] The sales rep reported that there was an infection approximately 1 week post-op. The patient was treated with antibiotics and the infection has resolved. There is no revision planned. No sterilization records are available. There is no known history of infection at the facility. This is report 1 of 2 as two separate devices were implanted at the same time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009582362-2018-00004
MDR Report Key7704859
Date Received2018-07-19
Date of Report2018-07-19
Date of Event2018-06-28
Date Mfgr Received2018-06-28
Device Manufacturer Date2018-06-05
Date Added to Maude2018-07-19
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 ContactBETH PASHKO
Manufacturer StreetPO BOX 585 30 SOUTH SATELLITE ROAD
Manufacturer CitySOUTH WINDSOR CT 06074
Manufacturer CountryUS
Manufacturer Postal06074
Manufacturer Phone8606569450
Manufacturer G1OXFORD PERFORMANCE MATERIALS
Manufacturer StreetPO BOX 585 30 SOUTH SATELLITE ROAD
Manufacturer CitySOUTH WINDSOR CT 06074
Manufacturer CountryUS
Manufacturer Postal Code06074
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHTR-PEKK
Generic NameFACIAL IMPLANT
Product CodeKKY
Date Received2018-07-19
Model NumberPK620898
Lot Number202442-001
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerOXFORD PERFORMANCE MATERIALS
Manufacturer AddressPO BOX 585 30 SOUTH SATELLITE ROAD SOUTH WINDSOR CT 06074 US 06074


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-07-19

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