FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Transcervical Contraceptive Tubal Occlusion Device
PMA: P020014
·
Supplement: S034
·
Decision Jul 1, 2011
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
- S034
- 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
- July 1, 2011
- Date Received
- April 12, 2011
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO REMOVE A CONTRAINDICATION AND TO REVISE A WARNING REGARDING NICKEL SENSITIVITY IN PHYSICIANS LABELING.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HHS | Transcervical Contraceptive Tubal Occlusion Device | FDA class 3 | Obstetrics/Gynecology |