General & Plastic Surgery 15
- Testing of Tissue Containment Systems Used During Power Morcellation Procedures
- Labeling Requirements for Surgical Staplers and Staples for Internal Use
- Product Labeling Requirements for Laparoscopic Power Morcellators in Gynecologic Surgery
- Regulatory Considerations for Microneedling Devices Used in Aesthetic Skin Treatments
- Breast Implants - Premarket Requirements for Saline and Silicone Gel-Filled Devices
- Breast Implant Labeling: Patient Communication and Risk Information Requirements
- Testing and Performance Requirements for Electrosurgical Devices and Accessories for General Tissue Cutting and Coagulation
- 510k Exemption for Unclassified Medical Devices in Selected Product Categories
- Labeling Requirements for Ultrasonic Surgical Aspirator Devices - Contraindication for Uterine Fibroid Procedures
- Evaluation and Reporting of Age, Race, and Ethnicity Data in Medical Device Clinical Studies
- Procedures for Medical Devices Advisory Committee Panel Meetings
- Bipolar Electrosurgical Vessel Sealers for General Surgery - Performance Testing and Labeling Requirements
- Assessment of Radiofrequency-Induced Heating in Multi-Configuration Passive Medical Devices for MR Conditional Labeling
- Clinical Trial Design and Regulatory Considerations for Nail Appearance and Onychomycosis Treatment Devices
- Applying Human Factors Engineering and Usability Engineering to Medical Devices