BIO Medical, Healthcare Institutions, Life Sciences, Regulatory Focus News Letter

FDA Issues Draft Guidance on Performance Criteria for Magnetic Resonance (MR) Coils

Hi, Welcome to FWQRC Regulatory Focus News letter

Greetings from FWQRC………..

Here we are going to discuss about the recent draft guidance on performance criteria for MR Coils

Facts about the draft guidance
This draft guidance is intended to provide performance criteria for magnetic resonance (MR) coils in support of the Safety and Performance Based Pathway.

Under the Safety and Performance Based Pathway, medical device manufacturers planning to submit a 510(k) will have the option to use the performance criteria as identified in a final guidance to support substantial equivalence, rather than direct comparison of the performance of the subject device to that of a predicate device.

What is MR Coils

MAGNETIC RESONANCE IMAGING

Framework for the Safety and Performance Based Pathway
Overview
There are three types of Premarket Notification 510(k)s that may be submitted to FDA: Traditional; Special; and Abbreviated. The Special and Abbreviated 510(k) programs were developed in 1998 and described in the “New 510(k) Paradigm” to facilitate the 510(k) review process for certain types of submissions subject to 510(k) requirements. In 2019, the FDA split “The New 510(k) Paradigm” into separate guidance documents; The Special 510(k) Program and The Abbreviated 510(k) Program. The Safety and Performance Based Pathway is an expansion of the concept of the Abbreviated 510(k) pathway for certain, well understood device types.
The FDA expects to operationalize this pathway once the first device types and applicable performance criteria have been identified and final guidances have been published. Once the FDA begins to operationalize this pathway, a medical device manufacturer will have the option to meet FDA-identified performance criteria to demonstrate that its device is as safe and effective as a predicate device. The use of this pathway does not affect the FDA’s ability to request any information authorized by the statute or regulations.

What device types are appropriate for the Safety and Performance Pathway?

The Safety and Performance Based Pathway is appropriate when FDA has determined that:

The new device has the same indications for use as, and technological characteristics that do not raise different questions of safety and effectiveness than the identified predicate; and

The new device meets all the FDA-identified performance criteria.

If any of the above factors are not met, the submitter has the option to submit a Traditional, Special or Abbreviated 510(k).

The FDA will issue future final guidance(s) to apply this Safety and Performance Based Pathway to certain types of devices with corresponding FDA-identified performance criteria. Industry and other stakeholders may suggest device types for which the FDA should consider identifying performance criteria. For example, industry may suggest devices for which there are comprehensive FDA-recognized consensus standards. We encourage industry and other stakeholders to submit evidence-based suggestions on what the performance criteria should be for eligible device types. Input can be provided using the docket number FDA-2018-D-1387 at http://www.regulations.gov.

The FDA intends to maintain a list of device types appropriate for the Safety and Performance Based Pathway on this website, accompanied by the guidance documents that identify the performance criteria for each device type, as well as the testing methods recommended in the guidances where feasible, and any other relevant information.

Content of a Safety and Performance Based 510(k)

The amount and type of information necessary to support a finding of substantial equivalence under the Safety and Performance Based Pathway will depend on the underlying source for the performance criteria and testing methods. Table 1 and the Appendix within the Safety and Performance guidance summarize the types of information that should be included in a submission based on the submitter’s approach. 

Importantly, 510(k) submitters still need to identify a predicate for certain aspects of substantial equivalence. However, instead of conducting direct comparison testing to demonstrate that a device is as safe and effective as a predicate device, manufacturers will have the option to use this pathway to demonstrate substantial equivalence, when appropriate.

More information on content that should be included within a Safety and Performance Based 510(k) will be available in the device-specific guidances that will be issued.

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