Infographic: Finding a Predicate for FDA 510(k) Submission

Navigating the 510(k) Pathway

Your expert guide to identifying the right predicate device for a streamlined FDA submission.

What is a Predicate Device?

A predicate device is a legally marketed U.S. device to which a new device is compared to establish "Substantial Equivalence." This is the cornerstone of a successful 510(k) submission, proving your device is as safe and effective as one already cleared by the FDA.

Substantial equivalence is determined by two critical factors:

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Same Intended Use

The new device must have the same purpose and be used in the same way as the predicate device.

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Similar Technological Characteristics

The device's technology, materials, and design must be the same, or any differences must not raise new safety or effectiveness concerns.

Predicate Strength is Key

A strong, well-justified predicate is the leading indicator of a successful 510(k) clearance.

The Predicate Search & Submission Pathway

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Step 1: Begin Your Search in FDA Databases

Utilize the 510(k) Premarket Notification and De Novo Classification databases.

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Step 2: Analyze Potential Predicates

Evaluate against key criteria to find the best fit.

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Suitable Predicate Found?

YES

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Proceed with 510(k) Submission

Build your submission around the chosen predicate to demonstrate substantial equivalence.

NO

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Consider De Novo Pathway

For novel, low-to-moderate risk devices with no existing predicate.

Deep Dive: How to Analyze Predicates

When examining a potential predicate's 510(k) summary, focus on these four critical areas to ensure the strongest possible comparison.

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Intended Use

This is the most critical factor. Is the intended use identical? Even small differences can disqualify a predicate.

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Tech Characteristics

Compare design, materials, energy sources, and mechanism of action. You must justify all differences.

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Performance Data

Review the required testing (bench, animal, clinical). This provides a roadmap for your own validation efforts.

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Clearance Date

The FDA prefers more recent predicates that reflect current technology and standards. Avoid very old predicates if possible.

A thorough predicate search is the first and most critical step in your regulatory strategy. It sets the stage for a predictable and successful journey to market.

Master Full USFDA submission 510k , PMA & De novo


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