Supera Peripheral Stent System, Supera Pro Interwoven Peripheral Stent System
FDA premarket approval P120020/S020 · decided 2018-10-04
Approval details
- PMA number
- P120020
- Supplement
- S020
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Supera Peripheral Stent System, Supera Pro Interwoven Peripheral Stent System
- Generic name
- STENT, SUPERFICIAL FEMORAL ARTERY
- Applicant
- Abbott Vascular (Idef Technologies Inc)
- Date received
- 2018-09-05
- Decision date
- 2018-10-04
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- NIP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Clara, CA
- Statement
- Increase the sterilization load density with a modified configuration.
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