On August 14, FDA issued a draft guidance regarding the evaluation of automatic class III designation, otherwise known as de novo classification. De Novo Number: DEN180005 . C. Measurand: Glucose in Interstitial Fluid A summary of devices and regulatory pathways can be seen in Table 1. <> DEN170022 . 8 0 obj The De Novo summary is intended to present an objective and balanced summary of the scientific evidence that served as the basis for the decision to grant a De Novo request. >> <> The Food and Drug Administration Modernization Act of 1997 (FDAMA) added the De Novo classification option as an alternate pathway to classify novel medical devices that had automatically … Evaluation of Automatic Class III Designation (De Novo) Summaries Media Contact: Megan McSeveney , 240-402-4514 Consumer Inquiries : DICE or 888-INFO-FDA E. Regulatory Information . >> The purpose of this document is to provide FDA's proposals for guidance to FDA staff and industry on the process for the submission and review of petitions submitted under the Evaluation of Automatic Class III Designation section of the Federal Food, Drug, and Cosmetic Act (the FD&C Act), also known as the de novo classification process. DRAFT GUIDANCE . Purpose for Submission: De Novo request for evaluation of automatic class III designation for Control-IQ technology. A. The guidance details a recent change in the requirements for submitting de novo classification request. /Annots [<> endobj B. endobj >> <> EVALUATION OF AUTOMATIC CLASS III DESIGNATION FOR Dexcom G6 Continuous Glucose Monitoring System . >> <> A. DEN Number . The .gov means it’s official.Federal government websites often end in .gov or .mil. A. DEN Number: DEN190034 . Psychological evaluation. Evaluation of Automatic Class III Designation (De Novo) Summaries. This guidance replaces “New Section 513(f)(2) – Evaluation of Automatic Class III Designation, Guidance for … DECISION SUMMARY . These may include, for example, a complete blood count (CBC), a check of your thyroid function, and screening for alcohol and drugs. C. Applicant . Purpose for Submission: De novo request for evaluation of automatic class III designation for Imagen Technologies, >> <> Document issued on: August 14, 2014 2. EVALUATION OF AUTOMATIC CLASS III DESIGNATION FOR MSK-IMPACT (Integrated Mutation Profiling of Actionable Cancer Targets) DECISION SUMMARY A. DEN Number: DEN170058 B. EVALUATION OF AUTOMATIC CLASS III DESIGNATION (DE NOVO) FOR ARGO REWALK™ REGULATORY INFORMATION FDA identifies this generic type of device as: Powered Exoskeleton. Under this program, products are automatically classified as Class III devices, despite their overall safety and effectiveness. related to the De Novo classification process, including what information to submit when seeking a path to market via the De Novo classification process. FDA 23andMe Personal Genome Service (PGS) Test – Evaluation of Automatic Class III Designation – De Novo Request (Memorandum) Grants FDA approval to the 23andMe Personal Genome Service (PGS) test as a Class II medical device for ten diseases and conditions and outlines special controls to mitigate risks involved. This includes discussing your thoughts, feelings, symptoms and behavior patterns. Option 2: Any person who determines that there is no legally marketed device upon which to base a determination of substantial equivalence may submit a De Novo request for the FDA to make a risk-based classification of the device into Class I or II, without first submitting a 510(k) and receiving an NSE determination. Therefore, we request revision of OMB control number 0910-0844, “De Novo Classification Process (Evaluation of Automatic Class III Designation)” to include the Acceptance Checklist and the Recommended Content Checklist in the hourly burden estimate for De Novo requests. An official website of the United States government, : A coversheet clearly identifying the request as a “Request for Evaluation of Automatic Class III Designation” under 513(f)(2) or De Novo request. assessing whether a request for an evaluation of automatic class III designation (De Novo classification request or De Novo request) meets a minimum threshold of acceptability and should be accepted for substantive review. Devices that are classified through the de novo process may be marketed and used as predicates for future 510(k) submissions. >> EVALUATION OF AUTOMATIC CLASS III DESIGNATION FOR QuantX . Steps to help diagnose OCD may include: 1. De Novo Classification. B. DECISION SUMMARY . Physical exam. Purpose for Submission: De Novo request for evaluation of automatic class III designation for the Dexcom G6 Continuous Glucose Monitoring System . %PDF-1.4 <> <> stream 3. >> <> %���� Evaluation of Automatic Class III Designation (De Novo) APPLICATION CORRESPONDENT (e.g., consultant, if different from above) FORM FDA 3514 (6/05) PSC Media Arts (301) 443-1090 EF PMA PMA & HDE Supplement Establishment Registration Number (if known) Original Submission PDP 510(k) Humanitarian Device Other Submission Exemption (HDE) Amendment Quantitative Insights, Inc. D. Proprietary and Established Names . The Food and Drug Administration Modernization Act of 1997 (FDAMA) added the de novo classification option as an alternate pathway to classify novel devices of low to moderate risk that had automatically been placed in Class III after receiving a â€œnot substantially equivalent” (NSE) determination in response to a premarket notification [510(k)] submission. Such devices are termed “de novo” devices and are managed much like devices with predicates in a less rigorous process. You can use an alternative approach if it satisfies the requirements of the applicable statutes and regulations. Purpose for Submission . >> <> This guidance document is being distributed for comment purposes only. Purpose for Submission: De novo request for evaluation of automatic class III designation for the MSK-IMPACT C. Measurand: 10 0 obj /Contents 16 0 R The De Novo summary also serves as a resource regarding the types of information necessary to support substantial equivalence for device manufacturers that may wish to use the device as a predicate for future 510(k) submissions. 1. QuantX . >> <> Evaluation of Automatic Class III Designation (De Novo) Summaries Media Contact: FDA Office of Media Affairs, 301-796-4540 Consumer Inquiries : Email or 888-INFO-FDA 3Y�O�s������Pڠ�СQ�W�����L$S>�� �:�Gm����4&و�u�����B/-=���f��8���uh�]�n��ڴ@��9�)�#��.P�n҄6 �xဆ����ѐ���~����r\(��M�)�^�۽��ŋ�>]���W�p��t���>۠沛�g�6dSo��eKiz� �p�mf�8�\�����g�Z�1�v��u��Y�Tl����R�B[j�,O�y\E^�t���L��_]=4+4+B�^h����!Z�7�YيV�@hVhV�h��L�kh�^�V��֊�.�hV�О?�m��Z�͊�n�l�[�WKK��jo�]����һ��ի�ϟF[5�B[{6�*\[����^��e��pmqh+GG�uFl�6]����.���!ޅ�OI�o�����Sy��>|-p�>T�S#Çj~ꡯ_�z�KEƸ|��=���.�aS�y.m�;�B�����Tw����N����%�_ՙ�~Ug~�5����z�Vs^��j�+�_�i��k���n-�֯�F�՜w�����r�K�jλ�_�i��k��zn-?��C>|���}����y{�6�s�ĻJp�H������\+O�,�6��[eK��j��++�X��$A��ku}� u��v����2�᧵o������T���y����G��3o��O���h%�;ݎ��. A coversheet clearly identifying the request as a "Request for Evaluation of Automatic Class III Designation" under 513 (f) (2) De Novo request. Before sharing sensitive information, make sure you're on a federal government site. Links to all available De Novo summary documents can be found in the table below. De Novo classification, also known as Evaluation of Automatic Class III Designation, is a risk-based classification process of novel devices for which there are no legally marketed predicate devices. Table 1. FDA’s initial volley on this issue came in the form of its 2014 draft guidance, de novo Classification Process (Evaluation of Automatic Class III Designation). >>] Focusing the Agency’s review resources on complete De Novo requests will provide a more Substantially Equivalent 510(k) Device Information, Recalls, Market Withdrawals and Safety Alerts, Substantially Equivalent 510(k) Device Information, Evaluation of Automatic Class III Designation (De Novo) Summaries (CBER), Sepax Cell Separation System and single use kits, TRUEGENE HIV-1 Genotyping Kit and OpenGene DNA Sequencing System, De Novo Classification Process (Evaluation of Automatic Class III Designation) - Guidance for Industry and Food and Drug Administration Staff, User Fees and Refunds for De Novo Classification Requests - Guidance for Industry and Food and Drug Administration Staff, FDA and Industry Actions on De Novo Classification Requests: Effect on FDA Review Clock and Goals - Guidance for Industry and Food and Drug Administration Staff, Acceptance Review for De Novo Classification Requests - Guidance for Industry and Food and Drug Administration Staff, Factors to Consider When Making Benefit-Risk Determinations in Medical Device Premarket Approval and De Novo Classifications - Guidance for Industry and FDA Staff, Evaluation of Automatic Class III Designation (De Novo) Summaries, Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions. EVALUATION OF AUTOMATIC CLASS III DESIGNATION FOR Control-IQ Technology DECISION MEMORANDUM . EVALUATION OF AUTOMATIC CLASS III DESIGNATION FOR OSTEODETECT. The Food and Drug Administration Modernization Act of 1997 (FDAMA) added the de novo classification option as an alternate pathway to classify novel devices of low to moderate risk that had automatically been placed in Class III after receiving a “not substantially equivalent” (NSE) determination in response to a premarket notification [510(k)] submission. De novo request for evaluation of automatic class III designation for QuantX. SUMMARY: The Food and Drug Administration (FDA or Agency) ... "De Novo Classification Process (Evaluation of Automatic Class III Designation) "De Novo classification process 0910-0844 800, 801, and 809 Medical Device Labeling Regulations 0910-0485 >> <> B. GUIDANCE DOCUMENT. The draft guidance entitled “De Novo Classification Process (Evaluation of Automatic Class III Designation)” provides guidance on the process for the submission and review of a De Novo classification request (hereafter a “De Novo request”) under section 513(f)(2) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. Since 2010, the FDA has begun releasing summary documents for devices classified through the De Novo process. Automatic Class III designation (de novo classification) The Food and Drug Administration Modernization Act of 1997 created section 513(f)(2) of the FD&C Act, which obligated the FDA to establish a risk-based regulatory system for medical devices. Evaluation of Automatic Class III Designation (De Novo) Summaries. >> <> Option 1: Any person who receives an NSE determination in response to a 510(k) submission may, within 30 days of receipt of the NSE determination, submit a De Novo request for the FDA to make a risk-based evaluation for classification of the device into Class I or II. A new type of device is automatically classified as class III, regardless of its risk, if no similar device exists to guide FDA in classifying it. /MediaBox [0 0 611 791] DECISION SUMMARY . B. 1. FDA 23andMe Personal Genome Service (PGS) Test – Evaluation of Automatic Class III Designation – De Novo Request (Memorandum) Grants FDA approval to the 23andMe Personal Genome Service (PGS) test as a Class II medical device for ten diseases and conditions and outlines special controls to mitigate risks involved. )&�+�k�����@��#tA�?9���G���������s��1N�Q�B="�����Z�<6=���֙SM�S��*s� Q���D�zఴ?��R��q�q�E���L�m9���l����,? Lab tests. It does not establish any rights for any person and is not binding on FDA or the public. De Novo Classification Process (Evaluation of Automatic Class III Designation) Draft Guidance for Industry and Food and Drug Administration Staff . The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. x���ݮ69o%v�W��@�KE����>N``.�{�7�x���RUIk=�ӝ����ͽJK�(�:~b,�����ߎ�� ���_���߬4ڊ�����������������˯�������_�_��X��{�a��M�o���?�s�K����T���/���o��qH�?~�����*�VY�B �4�qZw���C��X�O�|���_���D��x�1����/�������W��? De Novo Classification Process (Evaluation of Automatic Class III Designation) Guidance for Industry and Food and Drug Administration Staff October 2017 >> <> Class III devices are those considered high risk, therefore requiring the often lengthier Premarket Approval (PMA) process: this new de novo process was designed to usher through any new device that was both 1) unprecedented (novel), and 2) low … Duke SciPol, "FDA 23andMe Personal Genome Service (PGS) Test – Evaluation of Automatic Class III Designation – De Novo Request (Memorandum)" available at http://scipol.duke.edu/content/fda-23andme-personal-genome-service-pgs-test-%E2%80%93-evaluation-automatic-class-iii-designation-%E2%80%93 (10/24/2017). C. 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