Full Launch of Exactech’s Acapella One Cervical Spacer
Exactech commenced full launch of the Acapella® One Spacer, a cervical cage pre-assembled with integrated anchors to prevent device migration during anterior cervical fusion. Jun 20, 2016
First Patient Treated in Microbion’s Phase IIA Orthopaedic Infection Trial
Microbion enrolled the first patient in its U.S. Phase IIA study of MBN-101 candidate for treatment of orthopaedic implant-related infections. Jun 17, 2016
Spineology Launches Elite Expandable Interbody Fusion System
Spineology released the Elite™ Expandable Interbody Fusion system, designed to be implanted at a minimal height and expanded after final positioning in the disc space. Jun 17, 2016
OrthoPediatrics Files for $75MM IPO
OrthoPediatrics filed to raise up to US $75MM in an initial public offering. The company plans to list on the NASDAQ under the symbol KIDS. Pricing terms were not disclosed. Jun 17, 2016
Zimmer Biomet Enhances the OSS Orthopedic Salvage System
Zimmer Biomet commenced global launch of enhancements to its OSS™ Orthopedic Salvage joint reconstruction prostheses, designed to treat bone loss due to trama, tumor, multiple revision arthroplasties, etc. Jun 17, 2016
SpineGuard Receives 510(k) Clearance to Market PediGuard Threaded DSG
SpineGuard received FDA 510(k) clearance to market the PediGuard Threaded DSG™ device for Dynamic Surgical Guidance in pedicle screw insertion. Jun 16, 2016
Zimmer Biomet Reportedly Breached Deferred Prosecution Deal
Court filings suggest that Biomet breached a 2012 deferred prosecution agreement undertaken to resolve a foreign corruption investigation. Jun 15, 2016
SeaSpine Introduces Hollywood VI NanoMetalene Interbody Device
SeaSpine commenced full commercial launch of the Hollywood™ VI (variable insertion) NanoMetalene® device for transforaminal lumbar interbody fusion. Jun 15, 2016
Amendia Launches Ceres-C Standalone Cervical Interbody Device
Amendia commenced commercial launch of Ceres™-C, a low-profile standalone PEEK cervical interbody spacer designed for use in ACIF. Jun 15, 2016
Tyber Medical Expands FDA 510(k) Clearance of Headed and Snap-Off Screws
Tyber Medical received FDA 510(k) clearance of its headed and snap-off screws with configurations incorporating the proprietary BioTy™ modified surface treatment. Jun 15, 2016
