What does DSORD mean in SURGICAL
DSORD stands for Division of Surgical Orthopedic and Restorative Devices. It is a division within the Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration (FDA).
DSORD meaning in Surgical in Medical
DSORD mostly used in an acronym Surgical in Category Medical that means Division of Surgical Orthopedic and Restorative Devices
Shorthand: DSORD,
Full Form: Division of Surgical Orthopedic and Restorative Devices
For more information of "Division of Surgical Orthopedic and Restorative Devices", see the section below.
Responsibilities
DSORD is responsible for regulating medical devices related to:
- Surgical Procedures: Devices used in surgical interventions, such as bone saws, surgical drills, and electrocautery units.
- Orthopedics: Devices used for the treatment of musculoskeletal conditions, including bone plates, joint replacements, and spinal implants.
- Restorative Devices: Devices designed to restore function or improve quality of life, such as prosthetics, hearing aids, and pacemakers.
Functions
DSORD's primary functions include:
- Premarket Review: Evaluating the safety and effectiveness of medical devices before they are marketed.
- Postmarket Surveillance: Monitoring the performance of approved devices to identify any safety issues.
- Enforcement Actions: Taking regulatory actions against manufacturers or distributors who violate medical device regulations.
- Policy Development: Establishing policies and guidance on medical devices to ensure patient safety and innovation.
Essential Questions and Answers on Division of Surgical Orthopedic and Restorative Devices in "MEDICAL»SURGICAL"
What is the Division of Surgical Orthopedic and Restorative Devices (DSORD)?
The Division of Surgical Orthopedic and Restorative Devices (DSORD) is a division within the U.S. Food and Drug Administration (FDA) responsible for reviewing and regulating medical devices used in surgical, orthopedic, and restorative procedures.
What types of devices are regulated by DSORD?
DSORD regulates a wide range of devices, including:
- Implantable devices, such as artificial joints and spinal implants
- External fixation devices, such as casts and braces
- Surgical instruments, such as scalpels and forceps
- Anesthesia and respiratory devices
- Rehabilitation and assistive devices, such as wheelchairs and prosthetics
What is the role of DSORD in the medical device approval process?
DSORD plays a crucial role in ensuring the safety and effectiveness of medical devices used in surgical, orthopedic, and restorative procedures. The division reviews premarket submissions from device manufacturers to assess the devices' benefits and risks and determine whether they can be marketed and sold in the United States.
What factors does DSORD consider when reviewing medical devices?
DSORD considers several factors when reviewing medical devices, including:
- The intended use of the device
- The design and materials used in the device
- The potential risks and benefits associated with the device
- The results of clinical trials and other studies
- The manufacturing process and quality control procedures
How can I contact DSORD?
You can contact DSORD by phone at (301) 796-5341 or by email at [email protected].
Final Words: DSORD plays a critical role in ensuring the safety and effectiveness of medical devices used in surgical, orthopedic, and restorative procedures. By regulating these devices, DSORD helps protect the public health and promotes responsible innovation in the medical device industry.