DeviceClearance

Product code KNF— Obstetrics/Gynecology

Sonata Transcervical Fibroid Ablation System 2.2

Classification name
Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Device class
Class 2
Regulation
21 CFR 884.4160
Advisory panel
Obstetrics/Gynecology
Total cleared
44
First cleared
Most recent

Market context for product code KNF

FDA has cleared 44 devices under product code KNF between 1977 and 2025, filed by 30 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code KNF

Recent clearances under product code KNF

Data sourced from openFDA. This site is unofficial and independent of the FDA.