Resolute Integrity RX Coronary Stent System & Resolute Integrity OTW Cornary Stent System
FDA premarket approval P110013/S082 · decided 2017-10-13
Approval details
- PMA number
- P110013
- Supplement
- S082
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Resolute Integrity RX Coronary Stent System & Resolute Integrity OTW Cornary Stent System
- Generic name
- Coronary drug-eluting stent
- Applicant
- Medtronic Vascular
- Date received
- 2017-09-14
- Decision date
- 2017-10-13
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- NIQ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Rosa, CA
- Statement
- Changes to the work steps used in the manufacture of the bare metal stent.
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