Adiana Permanent Contraception System

FDA premarket approval P070022 · Laparoscopic contraceptive tubal occlusion device

PMA numberP070022

Approval

Applicant
Hologic, Inc.
Received
August 10, 2007
Decision date
July 6, 2009 (APWD)
Supplements
22, latest March 28, 2012
Product code
KNH – Laparoscopic Contraceptive Tubal Occlusion Device

Official FDA PMA record

Approval order statement

APPROVAL FOR THE ADIANA PERMANENT CONTRACEPTION SYSTEM. THE DEVICE IS INDICATED FOR WOMEN WHO DESIRE PERMANENT BIRTH CONTROL (FEMALE STERILIZATION) BY OCCLUSION OF THE FALLOPIAN TUBES.