KKY

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Product code: KKY
Device name: Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
Device class: Class 2
21 CFR: 21 CFR 878.3500
Medical specialty: General, Plastic Surgery
Marketing pathway: 510(K)
Flag: Implant
510(k) clearances (all years, FDA): 25 (all years; only the last 3 years are listed here)

Official FDA classification page: KKY

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