About FDA
CDRH Plan of Action for 510(k) and Science
Implementation of Recommendations from the 510(k) and Science Reports
The links below provide information on steps CDRH is taking to foster medical device innovation and assure the safety and effectiveness of medical technologies used in the United States.
The Summary and Overview of Comments and Next Steps below describes which recommendations from the August 2010 reports on the 510(k) program and CDRH's use of science in its decision-making we will implement.
The Summary is accompanied by a Plan of Action, which outlines 25 specific actions and accompanying timelines for completion or for reaching a milestone in 2011. These actions will make the 510(k) program a blueprint for smarter medical device oversight; one that drives innovation and brings important technologies to patients.
Information on Improving Pre-Market Programs
Plan of Action for Implementation of 510(k) and Science Recommendations (PDF - 130KB)Questions About the Plan of Action? Submit Here Initial Results of 510(k) Audit - Analysis of Not Substantially Equivalent (NSE) Determinations Medical Device Reporting (MDR) Rate in 510(k) Cleared Devices Using Multiple Predicates Analysis of Premarket Review Times Under the 510(k) Program Innovation Pathway Proposed Pilot Triage Program Unique Device Identification
Guidance and Standard Operating Procedures
Federal Register Notice: Standard Operating Procedure for Notice to Industry Letters Standard Operating Procedure for "Notice to Industry" Letters (PDF - 66KB)CDRH Guidance Development SOP (PDF - 165KB)SOP: Decision Authority for Additional or Changed Data Needs for Premarket Submissions (Withdrawn) Guidance for Industry and FDA Staff - 510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device Draft Guidance for Industry, Clinical Investigators, Institutional Review Boards, and Food and Drug Administration Staff - FDA Decisions for Investigational Device Exemption (IDE) Clinical Investigations Draft Guidance for Industry and Food and Drug Administration Staff - De Novo Classification Process (Evaluation of Automatic Class III Designation) Guidance for Industry and Food and Drug Administration Staff - Factors to Consider When Making Benefit-Risk Determinations in Medical Device Premarket Approvals and De Novo Classifications Draft Guidance for Industry, Clinical Investigators, and Food and Drug Administration Staff - Design Considerations for Pivotal Clinical Investigations for Medical Devices SOP: Management of Review Staff Changes During the Review of a Premarket Submission Draft Guidance for Industry and Food and Drug Administration Staff - The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)] Draft Guidance for Industry and Food and Drug Administration Staff - CDRH Appeals Processes Draft Guidance for Industry and Food and Drug Administration Staff - Medical Device Classification Product Codes Guidance for Industry and FDA Staff - Factors to Consider When Making Benefit-Risk Determinations in Medical Device Premarket Approval and De Novo Classifications (PDF - 523KB)Draft Guidance for Industry and FDA Staff Medical Devices: The Pre-Submission Program and Meetings with FDA Staff
CDRH Center Science Council (CSC)
The CSC provides oversight of the Center’s science programmatic functions and helps share knowledge throughout the Center, consistent with CDRH’s other ongoing efforts to improve internal communication, consistency, transparency, and quality in scientific decision making, and predictability of regulatory pathways and requirements.
Network of Experts
The Food and Drug Administration (FDA) is announcing the availability of the standard operating procedure (SOP) for “Network of Experts.” The SOP describes the Center for Devices and Radiological Health’s (CDRH) process to provide CDRH staff with rapid access to scientific, engineering, and medical expertise when it is needed to supplement existing knowledge and expertise within the Center.
Network of Experts- Expert Utilization Standard Operating Procedure (DRAFT) Network of Experts - Expert Enrollment Standard Operating Procedure (DRAFT) Federal Register: Center for Devices and Radiological Health; Standard Operating Procedures for Network of Experts; Request for Comments FDA Outlines Plans for an Outside Network of Scientific Experts
Related Links
510(k) and Science Report Recommendations: Summary and Overview of Comments and Next Steps (PDF - 188KB)Letter From the Center Director (PDF - 43KB)FDA to improve most common review path for medical devices CDRH Preliminary Internal Evaluations -- Foreword: A Message from the Center Director (PDF - 243KB)CDRH Preliminary Internal Evaluations -- Volume I: 510(k) Working Group Preliminary Report and Recommendations (PDF - 1.8MB)CDRH Preliminary Internal Evaluations -- Volume II: Task Force Utilization of Science in Regulatory Decision Making Preliminary Report and Recommendations (PDF - 672KB)FDA Issues Assessments of the 510(k) Program and Use of Science in Decision-Making - Federal Register: CDRH 510(k) Working Group Preliminary Report and Recommendations, and Task Force on the Utilization of Science in Regulatory Decision Making Preliminary Report and Recommendations
CDRH Preliminary Internal Evaluations -- Basic Questions and Answers on Preliminary Reports