CORDIS SMART/ SMART CONTROL NITINOL STENT SYSTEM
FDA premarket approval P020036/S030 · decided 2014-10-23
Approval details
- PMA number
- P020036
- Supplement
- S030
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- CORDIS SMART/ SMART CONTROL NITINOL STENT SYSTEM
- Generic name
- STENT, ILIAC
- Applicant
- Cordis US Corporation
- Date received
- 2014-09-23
- Decision date
- 2014-10-23
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- NIO
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Miami Lakes, FL
- Statement
- CHANGES TO OPTIMIZE THE POUCH SEALING PROCESS AS WELL AS A NEW POUCH SEALER.
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