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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Abbott Medical Swift-Lock Anchor; SCS ANCHOR

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Abbott Medical Swift-Lock Anchor; SCS ANCHOR Back to Search Results
Model Number 1192
Medical Device Problem Code Fracture (1260)
Health Effect - Clinical Code Inadequate Pain Relief (2388)
Date of Event 08/14/2026
Type of Reportable Event Other
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Brand Name
Swift-Lock Anchor
Common Device Name
SCS ANCHOR
Manufacturer (Section D)
Abbott Medical
6901 preston rd
plano TX 75024
Manufacturer (Section G)
Abbott Medical
6901 preston rd
plano TX 75024
Manufacturer Contact
sara speyerer
6901 preston road
plano, TX 75024
+1(972)309-8000
MDR Report Key50811517
Report Number1627487-2026-10135
Device Sequence Number18786984
Product Code GZB
UDI-Device Identifier05415067024084
UDI-Public(01)05415067024084(10)7319788(17)220109
Combination Product (Y/N)N
Initial Reporter StateMN
Initial Reporter CountryUS
PMA/510(K) Number
K092371
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2020
Device Explanted Year2026
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) 09/17/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Operator of Device Health Professional
Device Expiration Date01/09/2022
Device Model Number1192
Device Catalogue Number1192
Device Lot Number7319788
Was Device Available for Evaluation? No
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 Date09/17/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured01/10/2020
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 SexFemale
Patient Weight140 LB
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