S.M.A.R.T. NITINOL STENT SYSTEM & S.M.A.R.T. CONTROL NITINOL STENT SYSTEM FOR USE IN LLIAC ARTERIES
FDA premarket approval P020036/S022 · decided 2012-02-06
Approval details
- PMA number
- P020036
- Supplement
- S022
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- S.M.A.R.T. NITINOL STENT SYSTEM & S.M.A.R.T. CONTROL NITINOL STENT SYSTEM FOR USE IN LLIAC ARTERIES
- Generic name
- STENT, ILIAC
- Applicant
- Cordis US Corporation
- Date received
- 2012-01-09
- Decision date
- 2012-02-06
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- NIO
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Miami Lakes, FL
- Statement
- USE OF NEW EQUIPMENT FOR THE UV BONDING PROCESS.
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