Cerene® Cryotherapy Device
FDA premarket approval P180032/S011 · decided 2023-01-17
Approval details
- PMA number
- P180032
- Supplement
- S011
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cerene® Cryotherapy Device
- Generic name
- Device, thermal ablation, endometrial
- Applicant
- Channel Medsystems, Inc.
- Date received
- 2022-12-21
- Decision date
- 2023-01-17
- Days to decision
- 27 days
- Decision code
- APPR
- Product code
- MNB
- Advisory committee
- Obstetrics/Gynecology
- Expedited review
- No
- Location
- Emeryville, CA
- Statement
- Approval for a modification to the manufacturing process to improve the PCB-to-battery tray solder joint for the Cerene Controller Board.
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