FDA PMA FDA Class 3 Approved 🇺🇸 United States

Transcervical Contraceptive Tubal Occlusion Device

PMA: P020014 · Supplement: S035 · Decision Mar 19, 2012
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
Transcervical Contraceptive Tubal Occlusion Device
Trade Name
CONCEPTUS ESSURE SYSTEM FOR PERMANENT BIRTH CONTROL
PMA Number
P020014
Supplement Number
S035
Device Class
FDA Class 3
Product Code
HHS
Generic Name
Transcervical contraceptive tubal occlusion device
Regulation Number
884.5380
Medical Specialty
Obstetrics/Gynecology
Advisory Committee
Obstetrics/Gynecology
Decision
Approved
Decision Code
APPR
Decision Date
March 19, 2012
Date Received
April 14, 2011
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR REVISED PROFESSIONAL AND PATIENT LABELING.

Classifications

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

Product Code Device Name
HHS Transcervical Contraceptive Tubal Occlusion Device