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.
Magnetic Compression Anastomosis System
General, Plastic Surgery
A magnetic compression anastomosis system is a surgical device used to create anastomoses in minimally invasive and laparoscopic gastrointestinal surgery by harnessing the polar attraction between magnet devices placed on tissue; compression and necrosis at the contact zone allow an anastomosis to form, after which the magnets are expelled naturally. It is classified as FDA Class II (510(k) required) under regulation 878.4816 in the General and Plastic Surgery specialty, with product code SAH. The device is not an implant, does not support life-sustaining functions, and does not include devices intended for weight loss or metabolic disease treatment.
510(k) Clearances
8 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.