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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MicroVention, Inc. Headway; Catheter, percutaneous

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MicroVention, Inc. Headway; Catheter, percutaneous Back to Search Results
Model Number MC272156S-CN
Medical Device Problem Code Material Protrusion/Extrusion (2979)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/27/2026
Type of Reportable Event Malfunction
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Brand Name
Headway
Common Device Name
Catheter, percutaneous
Manufacturer (Section D)
MicroVention, Inc.
35 enterprise
aliso viejo CA 92656
Manufacturer Contact
terrence callahan
35 enterprise
aliso viejo, CA 92656
+1(714)247-8000
MDR Report Key50793097
Report Number2032493-2026-08238
Device Sequence Number9607531
Product Code DQY
UDI-Device Identifier00811425021385
UDI-Public00811425021385
Combination Product (Y/N)N
Initial Reporter CountryCH
PMA/510(K) Number
K101542
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,User Facility,Company Representative,Distributor
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/16/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberMC272156S-CN
Device Lot Number0001580707
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer07/01/2026
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/27/2026
Initial Report FDA Received Date09/16/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured02/13/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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