KPK
- Product code
- KPK
- Device name
- Marker, Ostia, Aorto-Saphenous Vein
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4650
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (all years, FDA)
- 6 (all years; only the last 3 years are listed here)
Official FDA classification page: KPK
Classification and pathway per current FDA publications. Data from openFDA (CC0).