|
Device | ADIANA PERMANENT CONTRACEPTION SYSTEM |
Generic Name | Laparoscopic contraceptive tubal occlusion device |
Regulation Number | 884.5380 |
Applicant | HOLOGIC, INC. 250 Campus Drive Marlborough, MA 01752 |
PMA Number | P070022 |
Supplement Number | S008 |
Date Received | 11/19/2010 |
Decision Date | 05/05/2011 |
Withdrawal Date
|
10/23/2012 |
Product Code |
KNH |
Advisory Committee |
Obstetrics/Gynecology |
Supplement Type | 135 Review Track For 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL FOR REVISION OF WRIITEN WORK INSTRUCTIONS FOR A SOLDERING OPERATION. |