Quick Links: Skip to main page content
Skip to Search
Skip to Topics Menu
Skip to Common Links
U.S. Food & Drug Administration
Follow FDA
En Español
Search FDA
Home
Food
Drugs
Medical Devices
Radiation-Emitting Products
Vaccines, Blood & Biologics
Animal & Veterinary
Cosmetics
Tobacco Products
MAUDE Adverse Event Report: Houston Lead Model 304
FDA Home
Medical Devices
Databases
-
510(k)
|
DeNovo
|
Registration & Listing
|
Adverse Events
|
Recalls
|
PMA
|
HDE
|
Classification
|
Standards
CFR Title 21
|
Radiation-Emitting Products
|
X-Ray Assembler
|
Medsun Reports
|
CLIA
|
TPLC
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
08/31/2026
Type of Reportable Event
Malfunction
Search Alerts/Recalls
New Search
|
Submit an Adverse Event Report
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
houston, TX 77058
+1(281)667-2681
MDR Report Key
50904315
Report Number
1644487-2026-11141
Device Sequence Number
5903881
Product Code
LYJ
UDI-Device Identifier
05425025750139
UDI-Public
05425025750139
Combination Product (Y/N)
N
Initial Reporter State
TX
Initial Reporter Country
US
PMA/510(K) Number
P970003
Number of Events Summarized
1
Summary Report (Y/N)
N
Device Implanted Year
2022
Serviced by Third Party (Y/N)
N
Reporter Type
Manufacturer
Report Source
Health Professional,Company Representative
Initial Reporter Occupation
Physician
Type of Report
Initial
Report Date
(Section B)
09/25/2026
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 Date
01/12/2025
Device Model Number
304-20
Device Lot Number
6795
Was Device Available for Evaluation?
No
Is the Reporter a Health Professional?
Yes
Type of Report(Section G)
Thirty-Day
Initial Date Received by Manufacturer
08/31/2026
Initial Report FDA Received Date
09/25/2026
Was Device Evaluated by Manufacturer? (Y/N)
No
Date Device Manufactured
01/14/2021
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 Number
1
Patient Age
33 YR
Patient Sex
Female
-
-