FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Stent, Superficial Femoral Artery
PMA: P110023
·
Supplement: S065
·
Decision Feb 11, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Stent, Superficial Femoral Artery
- Trade Name
- EverFlex Self-Expanding Peripheral Stent System; EverFlex Self-Expanding Peripheral Stent with Entrust Delivery Syste
- PMA Number
- P110023
- Supplement Number
- S065
- Device Class
- FDA Class 3
- Product Code
- NIP
- Generic Name
- STENT, SUPERFICIAL FEMORAL ARTERY
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- February 11, 2026
- Date Received
- January 29, 2026
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
a new fixture used in the stent microblasting process
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NIP | Stent, Superficial Femoral Artery | FDA class 3 | Unknown |