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

Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)

K Number: K233848 · Decision Dec 21, 2023
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
43
Applicant Total
8
Review Days
16

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Basic Information

Device Name
Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)
K Number
K233848
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
884.4160
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gynesonics, Inc.
Date Received
December 5, 2023
Decision Date
December 21, 2023
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.

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Other Clearances by Gynesonics, Inc.

K Number Device Name
K250705 Sonata Transcervical Fibroid Ablation System 2.2
K240503 Sonata Transcervical Fibroid Ablation System 2.2
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