GENESYS HTA SYSTEM
FDA premarket approval P000040/S032 · decided 2014-06-10
Approval details
- PMA number
- P000040
- Supplement
- S032
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- GENESYS HTA SYSTEM
- Generic name
- Device, thermal ablation, endometrial
- Applicant
- Axora Medical, Inc.
- Date received
- 2014-05-14
- Decision date
- 2014-06-10
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- MNB
- Advisory committee
- Obstetrics/Gynecology
- Expedited review
- No
- Location
- Jacksonville, FL
- Statement
- QUALIFY AN ALTERNATE SECONDARY SUPPLIER OF THE TACKIFIER RESINS USED IN THE PRODUCTION OF THE COATINGS USED ON SHEATH AND CASSETTE TRAY TYVEK LIDS.
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