3.5MM POPLOK SUTURE ANCHOR CKP-3500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-19 for 3.5MM POPLOK SUTURE ANCHOR CKP-3500 manufactured by Conmed Corporation.

MAUDE Entry Details

Report Number1017294-2020-00137
MDR Report Key9856356
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-03-19
Date of Report2020-03-19
Date of Event2020-02-11
Date Mfgr Received2020-02-25
Date Added to Maude2020-03-19
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 ContactMS TRACEY WEISELBENTON
Manufacturer Street11311 CONCEPT BLVD
Manufacturer CityLARGO, FL
Manufacturer CountryUS
Manufacturer Phone3995557
Manufacturer G1CONMED CORPORATION
Manufacturer Street11311 CONCEPT BLVD
Manufacturer CityLARGO, FL
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3.5MM POPLOK SUTURE ANCHOR
Generic NameFASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE
Product CodeMBI
Date Received2020-03-19
Catalog NumberCKP-3500
Lot Number1047419
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONMED CORPORATION
Manufacturer Address11311 CONCEPT BLVD LARGO, FL US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-19

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