How do Orthopaedic Devices Change After Their Initial FDA Premarket Approval?
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Overview
publication date
- January 1, 2015
published in
has subject area
- Cross-Sectional Studies
- Databases, Factual
- Device Approval
- Equipment Design
- Humans
- Medical Device Recalls
- Orthopedic Equipment
- Orthopedic Procedures
- Patient Safety
- Product Surveillance, Postmarketing
- Retrospective Studies
- Risk Factors
- Safety-Based Medical Device Withdrawals
- Time Factors
- United States
- United States Food and Drug Administration