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.
Bone Fixation Cerclage, Sublaminar
Orthopedic
The Bone Fixation Cerclage, Sublaminar is an orthopedic implant that acts as a bone anchor for temporary stabilization or used in conjunction with other metallic medical implants when wiring is needed during development of a spinal fusion. It is classified as Class 2 (FDA Class 2), requiring 510(k) premarket clearance. The product code is OWI, with regulation number 888.3010 under the Orthopedic specialty, and it carries an implant flag indicating it is placed within the body.
510(k) Clearances
35 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.