KTW

Appliance, Fixation, Nail/Blade/Plate Combination, Single Component

Product code: KTW
Device name: Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
Device class: Class 2
21 CFR: 21 CFR 888.3030
Medical specialty: Orthopedic
Marketing pathway: 510(K)
Flag: Implant
510(k) clearances (all years, FDA): 38 (all years; only the last 3 years are listed here)

Official FDA classification page: KTW

Classification and pathway per current FDA publications. Data from openFDA (CC0).