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This document is a 510(k) summary submission to the FDA by Dentium Co., Ltd. for the SimpleLine II Abutment System, which is intended for use in dental prosthetic rehabilitation. It outlines the device's

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How to fill out 510(k) Summary

1. Identify the device you want to market and determine if it requires a 510(k).
2. Gather information on the predicate device(s) for comparison.
3. Prepare a summary of the device's technological characteristics.
4. Document the intended use and indications for the device.
5. Provide performance data to support safety and effectiveness.
6. Include labeling and promotional material.
7. Review and finalize the summary before submission.
8. Submit the 510(k) Summary to the FDA via the appropriate submission process.

Who needs 510(k) Summary?

1. Manufacturers of medical devices that seek to market their products in the U.S.
2. Companies looking to demonstrate that their device is substantially equivalent to a legally marketed device.
3. Startups and established companies introducing new or modified devices.

People Also Ask about

What are the three types of 510k?

There are three types of 510(k) submissions: Traditional, Abbreviated, and Special. Each type has its own requirements and may be appropriate for different types of medical devices. Traditional, Special, and Abbreviated 510(k)s require the same user fee.

What is the difference between 510k de novo and PMA?

PMA submissions are intended for high-risk devices, whereas De Novo and 510(k) are suitable for lower-risk devices with suitable predicates. Choosing the right submission pathway depends on various factors, including your device's risk level, the availability of predicates, and the resources you have available.

What are the different types of 510k s?

Types of 510(k)s. If your medical device is eligible under premarket notification criteria, there are three types of 510(k)s: Traditional, Abbreviated, and Special. The FDA offers separate checklists for the Traditional, Abbreviated, and Special 510(k)s in its Refuse to Accept Policy for 510(k)s guidance document.

What are class 1, class 2, and class 3 devices?

Class I (low to moderate risk): general controls. Class II (moderate to high risk): general controls and Special Controls. Class III (high risk): general controls and Premarket Approval (PMA)

What is the 510k pathway?

Section 510(k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to market a medical device at least 90 days in advance. This is known as Premarket Notification - also called PMN or 510(k).

What is the purpose of a 510 K to determine?

The focus of the 510(k) process is to prove something called 'substantial equivalence'. In other words, the aim of the game is to prove to the FDA that the medical device you want to bring to market is broadly similar to another device that's already on the market, known as a predicate device.

How long does 501k approval take?

Generally, 510(k) applicants can expect submission acceptance review decisions within 15 calendar days; substantive review decisions within 60 days; and final decisions within 90 days. Applicants with outstanding review issues will be notified within 100 days.

What is the difference between 510k cleared and approved?

When a medical device is cleared, this means it has undergone a 510(k) submission, which FDA has reviewed and provided clearance. Approval: For Class III medical devices to be legally marketed they must undergo a rigorous review and approval process.

For pdfFiller’s FAQs

What is 510(k) Summary?

A 510(k) Summary is a document submitted to the FDA that provides information about a medical device's safety and effectiveness, demonstrating how it is substantially equivalent to a legally marketed device.

Who is required to file 510(k) Summary?

Manufacturers of medical devices that are not exempt and wish to market a device in the U.S. must file a 510(k) Summary with the FDA before commercial distribution.

How to fill out 510(k) Summary?

To fill out a 510(k) Summary, manufacturers must provide details such as device identification, intended use, description, substantial equivalence information, labeling, and summary of performance data.

What is the purpose of 510(k) Summary?

The purpose of the 510(k) Summary is to demonstrate to the FDA that a new device is substantially equivalent to an existing device, thereby ensuring safety and effectiveness before it is marketed.

What information must be reported on 510(k) Summary?

The 510(k) Summary must report information such as the device name, model number, manufacturer details, intended use, technological characteristics, performance data, and any clinical or non-clinical studies.