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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HOUSTON LEAD MODEL 304

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HOUSTON LEAD MODEL 304 Back to Search Results
Model Number 304-20
Medical Device Problem Code Fracture (1260)
Health Effect - Clinical Codes Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/23/2026
Type of Reportable Event Malfunction
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Brand Name
LEAD MODEL 304
Common Device Name
LEAD
Manufacturer (Section D)
HOUSTON
100 cyberonics boulevard
houston TX 77058
Manufacturer (Section G)
HOUSTON
100 cyberonics boulevard
houston TX 77058
Manufacturer Contact
cindy scott
100 cyberonics blvd
suite 600
houston, TX 77058
2816672681
MDR Report Key25860570
Report Number1644487-2026-10860
Device Sequence Number20201424
Product Code LYJ
UDI-Device Identifier05425025750139
UDI-Public05425025750139
Combination Product (Y/N)N
Initial Reporter CountryCA
PMA/510(K) Number
P970003
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2022
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Nurse Practitioner
Type of Report Initial
Report Date (Section B) 07/17/2026
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 Lay User/Patient
Device Expiration Date05/17/2026
Device Model Number304-20
Device Lot Number7208
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 06/23/2026
Initial Report FDA Received Date07/17/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured05/23/2022
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 Age8 YR
Patient SexUnknown
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