Tool · 510(k)

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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: QBO FDA class 2

Instruments Designed For Press-Fit Osteochondral Implants

Orthopedic

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The Instruments Designed for Press-Fit Osteochondral Implants are orthopedic surgical instruments intended to manipulate bone and cartilage tissue or implant materials for the positioning, alignment, defect creation, or placement of press-fit osteochondral implants, used in cartilage repair procedures. It is classified as a Class 2 device under regulation 888.4505, subject to De Novo classification with general and special controls, and falls within the Orthopedic (OR) medical specialty. The product code is QBO. It is not an implant itself and is not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
Cartiva SCI instrumentation set
Cartiva SCI Disposable Instrumentation Set

What 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.

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