FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Thermal Ablation, Endometrial

PMA: P180032 · Supplement: S015 · Decision Nov 16, 2023
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Device, Thermal Ablation, Endometrial
Trade Name
Cerene® Cryotherapy Device
PMA Number
P180032
Supplement Number
S015
Device Class
FDA Class 3
Product Code
MNB
Generic Name
Device, thermal ablation, endometrial
Medical Specialty
Unknown
Advisory Committee
Obstetrics/Gynecology
Decision
Approved
Decision Code
APPR
Decision Date
November 16, 2023
Date Received
October 23, 2023
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for labeling changes that add and/or strengthen instructions that are intended to enhance the safe use of the device.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNB Device, Thermal Ablation, Endometrial