The approval is supported by data from 31 patients and 32 talus replacement surgeries. The Food and Drug Administration (FDA) has approved the Patient Specific Talus Spacer (Additive Orthopaedics) for ...
ENGLEWOOD, Colo.--(BUSINESS WIRE)-- Paragon 28, Inc. (NYSE: FNA) announced today that it has received a supplemental approval order from the U.S. Food and Drug Administration ("FDA") for the Patient ...
The FDA has approved its first 3D-printed metal implant designed to replace the main bone in the ankle joint connecting the leg to the foot. The agency issued a green light to New Jersey-based ...
Today, the U.S. Food and Drug Administration approved the Patient Specific Talus Spacer 3D-printed talus implant for humanitarian use. The Patient Specific Talus Spacer is the first in the world and ...
Avascular necrosis refers to the death of bone tissue that stems from an interruption in its blood supply. The condition typically affects the ends of long bones at weight-bearing joints, with the hip ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results