BioPoly Receives CE Mark for RS Partial Resurfacing Shoulder
BioPoly received approval under the CE Mark for the BioPoly® RS Partial Resurfacing Shoulder. ...
BioPoly received approval under the CE Mark for the BioPoly® RS Partial Resurfacing Shoulder. ...
On 4/20/16, FDA’s Orthopaedic and Rehabilitation Devices Panel will meet regarding the PMA for Cartiva’s Synthetic Cartilage Implant, an organic polymer-based biomaterial...
Cayenne Medical commenced U.S. launch of the BioWick™ SureLock™ implant, an interpositional scaffold wick designed to address the biology issue associated with...
Proxy Biomedical has developed high strength resorbable USP 2 suture for fracture and soft tissue repair applications. ...
FDA tentatively scheduled a 2Q16 meeting of the Orthopaedic and Rehabilitation Devices Panel to review Cartiva’s Premarket Approval Application for the Synthetic Cartilage Implant in...
Active Implants initiated SUN (Safety Using NUsurface®), a 2nd clinical trial evaluating the investigational meniscus implant....
Episurf Medical achieved a milestone of 100 accounts approved and connected to the company’s proprietary ?ifidelity™ IT platform, used with...
Episurf Medical received CE Mark approval for the Epioscopyâ„¢ Damage Assessment Tool, designed to support 3D visualization of knee segments,...
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