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.
Shoulder Arthroplasty Implantation System
Orthopedic
The Shoulder Arthroplasty Implantation System is a surgical instrument system designed to assist in the implantation of shoulder arthroplasty devices by guiding alignment, making or establishing cuts, and selecting, sizing, attaching, positioning, or orienting implant components. It is classified as FDA Class 2, meaning it requires a 510(k) premarket notification to demonstrate substantial equivalence to a predicate device. The product code is QHE, regulated under 21 CFR 888.3660, and falls under the Orthopedic medical specialty. It is not flagged as an implant or life-sustaining device, and is not exempt from Good Manufacturing Practices.
510(k) Clearances
22 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.