510(k) Predicate Finder
Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.
Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
General, Plastic Surgery
This material, consisting of polytetrafluoroethylene (PTFE) and vitreous carbon, is used in maxillofacial reconstructive surgery to repair or augment craniofacial bone defects, providing a biocompatible structural framework for facial reconstruction. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket clearance to demonstrate substantial equivalence. The product code is KKY and it is regulated under 21 CFR 878.3500 in the General and Plastic Surgery specialty. This device is an implant.
510(k) Clearances
25 matchesWhat is a Predicate Device?
A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.
Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.
Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.