Zimmer Biomet Enhances the OSS Orthopedic Salvage System
Zimmer Biomet commenced global launch of enhancements to its OSSâ„¢ Orthopedic Salvage joint reconstruction prostheses, designed to treat bone loss...
Zimmer Biomet commenced global launch of enhancements to its OSSâ„¢ Orthopedic Salvage joint reconstruction prostheses, designed to treat bone loss...
SpineGuard received FDA 510(k) clearance to market the PediGuard Threaded DSG™ device for Dynamic Surgical Guidance in pedicle screw insertion....
Court filings suggest that Biomet breached a 2012 deferred prosecution agreement undertaken to resolve a foreign corruption investigation....
SeaSpine commenced full commercial launch of the Hollywood™ VI (variable insertion) NanoMetalene® device for transforaminal lumbar interbody fusion....
Amendia commenced commercial launch of Ceres™-C, a low-profile standalone PEEK cervical interbody spacer designed for use in ACIF....
Tyber Medical received FDA 510(k) clearance of its headed and snap-off screws with configurations incorporating the proprietary BioTy™ modified surface treatment....
Strategic orthopaedic-related 510(k)s issued in May 2016 include:Â Navio Indication for TKA (Blue Belt Technologies), Enza Zero-profile Anterior Interbody Fusion System...
Bone Biologics signed an option agreement with UCLA for an opportunity to exclusively license the use of Nell-1 bone growth factor...
KB Medical received approval under the CE Mark for its AQrateâ„¢ Robotic Assistance system, indicated for use in general spinal...
Zimmer Biomet acquired Compression Therapy Concepts, provider of devices to prevent deep venous thrombosis following a variety of surgical procedures. CTC...
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