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.
Implant, Muscle, Pectoralis
Ear, Nose, Throat
The Pectoralis Muscle Implant is a surgically placed silicone or other biocompatible material device used for cosmetic or reconstructive augmentation of the pectoral region, typically to improve the contour and appearance of the chest in patients who have undergone surgery or have congenital anomalies. Classified as a Class 2 implantable device under 21 CFR 874.3620 within the Ear, Nose, and Throat specialty, it requires 510(k) premarket notification. It carries an implant flag, denoting its surgically implanted nature.
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.