FDA Pilot Program Helps Manufacturers Streamline Approval of Medical Devices

//FDA Pilot Program Helps Manufacturers Streamline Approval of Medical Devices

FDA Pilot Program Helps Manufacturers Streamline Approval of Medical Devices

Mesh Medical Device News Desk, September 18, 2017 ~ The FDA spends much of its resources working with device and drug manufacturers to help ease their way to market.

Here is another example of a newly announced pilot program that will help do just that. 

Unlike drugs, high-risk medical devices, even some permanently implanted, make it market with relative ease.

Now the U.S. Food and Drug Administration (FDA) is launching a pilot program that aims to further streamline the premarket approval (PMA) process for some high-risk medical devices.

Published in the Federal Register, the FDA’s Center for Devices and Radiological Health (CDRH) will solicit nine companies to join a pilot program called Premarket Approval Application Critical to Quality (PMA CtQ). The program will run from September 29, 2017 until the end of December 2018.

Flexible Endoscope medical device

The “FDA intends to work with each participating applicant to identify characteristics of its device and its manufacture that are critical to its quality, which may include specific device features or quality control practices. The identified CtQ characteristics and controls will help focus FDA’s post-approval inspection approach.”

Applicants would not be subject to pre-approval inspections of the medical devices, design and manufacture but instead focus on post-approval inspection.

There is no word in the Federal Register how an inspection could be conducted on an already implanted medical device or what the remedy would be if a design failure is determined post-market.

The agency says focusing on these activities would lead to fewer device failures, a decrease in device recalls, improved device innovation and efficiency and a streamlined inexpensive pathway to the market.

This is the latest example of FDA innovations that help device manufacturers get their devices to market faster under the “least burdensome” standard.

Upward of 95% of medical devices take the superhighway to the market through the FDA’s 510(k) clearance process (named for Section 510(k) of the Federal Food, Drug, and Cosmetic Act), after about 90 days, an exchange of paperwork, and a few thousand dollars.

That includes implantable medical device such as hernia mesh, transvaginal mesh, morcellator devices, hip implants, heart valve rings, and defibrillator leads, among other devices. See this Mesh News Desk story on medical devices that bypassed FDA scrutiny.

Patients and policymakers have long complained the clearance process does little to ensure medical devices are safe and effective.

Meanwhile the medical device industry complains that even the 510(k) is too burdensome and time-consuming and delays the launch of important new medical devices.

The 510 (K) process has long been scrutinized. In 2011 the Institute of Medicine called the clearance process “fatally flawed” and called for the outdated process to be abolished.  ###

By | 2017-09-18T00:24:03+00:00 September 18th, 2017|FDA News|5 Comments

About the Author:

I’m National News Editor, Jane Akre and I began Mesh Medical Device News Desk aka Mesh News Desk (MND) in the summer of 2011 just after the Food and Drug Administration issued an explicit warning to the public that complications associated with surgical mesh used for prolapse repair (POP) and incontinence (SUI) are NOT rare! That was the starting point for the litigation you see today and thousands of lawsuits have been filed by women whose lives have been altered, some permanently, by the use of this petroleum-based product.


  1. Bejah Blue September 19, 2017 at 7:09 pm - Reply

    This is deeply disturbing but not at all surprising. It is the kind of thing I have come to expect from our government. If any of us had any doubts about the failure of this government to care for its own people surely those have evaporated now. What “they do not seem to understand is that such behavior will lead to the end of the American dream, the death of the democratic ideal, the America we pledged allegiance to for so long. And if our America falls what do they think will happen to the world? Darkness falls…


    • Kitty September 21, 2017 at 4:52 pm - Reply

      You are so introspective Bejah. They will do or say anything for $. The ad that really disturbs me is the Grandma turning into a wolf…””keep your baby away because Gramma may give her WHOOPING COUGH.

      • Bejah Blue September 28, 2017 at 11:19 pm - Reply

        Kitty, Sounds horrible, I did not see that…maybe it was pulled. Bejah

        I hope everyone knows that at one time Jane posted a long list of Johnson & Johnson products so we would know what NOT to buy any longer. Please everyone go look for it, print it and keep it with you when you shop. We must stop buying their products. We must encourage all companies we do business with to STOP buying Jnj products also.

  2. Anna Daniel September 28, 2017 at 5:16 pm - Reply

    Dear Jane
    No new information on my tvt-mesh
    My question: Can I go to a website
    in which I will be able to see status of
    my case via the docket number
    and venue…if you can direct me
    here it will be more than appreciated
    My case is in Bergen County, in New Jersey

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