ADIANA PERMANENT CONTRACEPTION SYSTEM
FDA premarket approval P070022/S028 · decided 2012-03-28
Approval details
- PMA number
- P070022
- Supplement
- S028
- Supplement type
- 30-Day Notice
- Trade name
- ADIANA PERMANENT CONTRACEPTION SYSTEM
- Generic name
- Laparoscopic contraceptive tubal occlusion device
- Applicant
- Hologic, Inc.
- Date received
- 2012-03-01
- Decision date
- 2012-03-28
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- KNH
- Advisory committee
- Obstetrics/Gynecology
- Expedited review
- No
- Location
- Malborough, MA
- Statement
- MINOR CHANGES TO THE MANUFACTURING PROCEDURE OF THE CATHETER TIP FOR THE DEVICE.
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