FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Sonata Transcervical Fibroid Ablation System 2.2

K Number: K240503 · Decision Jul 17, 2024
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
43
Applicant Total
8
Review Days
147

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Sonata Transcervical Fibroid Ablation System 2.2
K Number
K240503
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gynesonics, Inc.
Date Received
February 21, 2024
Decision Date
July 17, 2024
Product Code
KNF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNF), ordered by most recent decision date.

View all

Other Clearances by Gynesonics, Inc.

K Number Device Name
K250705 Sonata Transcervical Fibroid Ablation System 2.2
K233848 Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)
K222304 Sonata Transcervical Fibroid Ablation System 2.2
K211535 Sonata Transcervical Fibroid Ablation System 2.2
K193516 Sonata® Sonography-Guided Transcervical Fibroid Ablation System 2.1
K173703 Sonata Sonography-Guided Transcervical Fibroid Ablation System
K061153 GYNESONICS EC6 TRANSDUCER