|Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.|
|Trade Name||ADIANA PERMANENT CONTRACEPTION SYSTEM|
|Classification Name||device, occlusion, tubal, contraceptive|
|Supplement Type||30-day notice|
|Supplement Reason|| process change: manufacturing|
|Expedited Review Granted?|| No|
|Approval Order Statement |
Addition of incoming inspection requirements to the plastic tubing used in the matrix molding process.