fda-consultant-specialist

Topics in the source

• FDA Consultant Specialist
• Table of Contents
• FDA Pathway Selection
• Decision Framework
• Pathway Comparison
• Pre-Submission Strategy
• 510(k) Submission Process
• Workflow

FDA regulatory consulting for medical device manufacturers covering submission pathways, the Quality Management System Regulation (QMSR, 21 CFR Part 820 — formerly the QSR), HIPAA compliance, and device cybersecurity requirements. FDA Pathway Selection 510(k) Submission Process QMSR Compliance (formerly QSR) HIPAA for Medical Devices Device Cybersecurity Resources -- Determine the appropriate FDA regulatory pathway based on device classification and predicate availability. | Pathway | When to Use | Timeline | User Fee (FY2024) | |---------|-------------|----------|-------------------| | 510(k) Traditional | Predicate exists, design changes | 90 days | $21,760 (FY2024) | | 510(k) Special | Manufacturing changes only | 30 days | $21,760 (FY2024) | | 510(k) Abbreviated | Guidance/standard conformance | 30 days | $21,760 (FY2024) | | De Novo | Novel, low-moderate risk | 150 days | $134,676 (FY2024) | | PMA | Class III, no predicate | 180+ days | $425,000+ (FY2024) | User fees are set annually under MDUFA. Verify current-fiscal-year fees at fda.gov (MDUFA user fee schedule) before budgeting; small-business rates differ. 1. Identify product code and classification 2. Search 510(k) databa

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