RESOLUTE INTEGRITY ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
FDA premarket approval P110013/S014 · decided 2013-07-10
Approval details
- PMA number
- P110013
- Supplement
- S014
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- RESOLUTE INTEGRITY ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
- Generic name
- Coronary drug-eluting stent
- Applicant
- Medtronic Vascular
- Date received
- 2013-05-28
- Decision date
- 2013-07-10
- Days to decision
- 43 days
- Decision code
- OK30
- Product code
- NIQ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Rosa, CA
- Statement
- UPGRADE TO THE SPRAY WEIGH AUTOMATED SYSTEM (SWAT III) AND SPRAYER CURRENTLY USED ON THE RESOLUTE INTEGRITY AND ENDEAVOR SPRINT DEVICES.
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