KWP
- Product code
- KWP
- Device name
- Appliance, Fixation, Spinal Interlaminal
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3050
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 430
Official FDA classification page: KWP
Classification and pathway per current FDA publications. Data from openFDA (CC0).