FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Thermal Ablation, Endometrial

PMA: P010013 · Supplement: S042 · Decision Dec 20, 2011
Classifications
1
FEI Numbers
19
Registration Numbers
19

Basic Information

Device Name
Device, Thermal Ablation, Endometrial
Trade Name
NOVASURE IMPENDANCE CONTROLLED ENDOMETRIAL ABLATION SYSTEM
PMA Number
P010013
Supplement Number
S042
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
December 20, 2011
Date Received
November 8, 2011
Supplement Type
Real-Time Process
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A CHANGE TO THE NOVASURE TO ADD THE SURESOUND UTERINE SOUND TO THE EXISTING THERMOFORMED TRAY FOR THE NOVASURE DISPOSABLE 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