FDA Adverse Event Injury Summary report: N

SONATA TRANSCERVICAL FIBROID ABLATION SYSTEM

MDR report key: 22952756 · Received September 3, 2025

Report

Report Number
3005875675-2025-00028
Event Type
Injury
Date Received
September 3, 2025
Date of Event
December 31, 2018
Report Date
September 3, 2025
Manufacturer
GYNESONICS
Product Code
KNF
UDI-DI
10817929020333
PMA / PMN Number
K173703
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THERE WAS NO REPORT OF DEVICE MALFUNCTION DURING THE PROCEDURE AND THE SYSTEM FUNCTIONED AS EXPECTED. SUBMISSION OF THIS REPORT IS ASSOCIATED WITH THE RECENT ACQUISITION OF GYNESONICS BY HOLOGIC, INC. DURING THE INTEGRATION INTO HOLOGIC'S ADVERSE EVENT REPORTING SYSTEM AND PROCEDURES, A REVIEW OF HISTORICAL ADVERSE EVENTS WAS PERFORMED. AS A RESULT, THIS EVENT WAS IDENTIFIED AS BEING REPORTABLE ON (B)(6) 2025 AND IS BEING REPORTED RETROACTIVELY OUT OF AN ABUNDANCE OF CAUTION.

Description of Event or Problem · 0

ON SEPTEMBER 24, 2019, IT WAS INITIALLY REPORTED TO GYNESONICS THAT A PATIENT TREATED WITH THE SONATA SYSTEM ON (B)(6) 2018. DURING TREATMENT SHE ALSO UNDERWENT HYSTEROSCOPIC MYOMECTOMY. ON (B)(6) 2018 THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR EMERGENCY TREATMENT FOR METRORRHAGIA GRAVIS [UTERINE BLEEDING AT IRREGULAR INTERVALS, PARTICULARLY BETWEEN THE EXPECTED MENSTRUAL PERIODS]. THE DOCTOR PERFORMED OPERATIVE HYSTEROSCOPY WITH FIBROID RESECTION. THE PATIENT WAS DISCHARGED ON (B)(6) 2019.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1733915 SONATA TRANSCERVICAL FIBROID ABLATION SYSTEM ULTRASOUND-GUIDED INTRAUTERINE RADIO-FREQUENCY ABLATION SYSTEM KNF GYNESONICS SONATA-240 10817929020333

Patients

Seq Age Sex Outcome Treatment
1 NA Female Required Intervention| H HYSTEROSCOPIC MYOMECTOMY