STELID II BTF/BJF - STELIX II BRF
FDA premarket approval P020030/S010 · decided 2013-10-02
Approval details
- PMA number
- P020030
- Supplement
- S010
- Supplement type
- 30-Day Notice
- Trade name
- STELID II BTF/BJF - STELIX II BRF
- Generic name
- Permanent defibrillator electrodes
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2013-09-11
- Decision date
- 2013-10-02
- Days to decision
- 21 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- CHANGE TO THE ROUTINE BIOBURDEN MONITORING BEFORE STERILIZATION.
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