Greatbatch has received FDA pre-market approval for its Algovita spinal cord stimulation system, according to a Mass Device report.
Spinal Tech
PolyPid enrolled the first patient in its clinical trial of BonyPid-1000.
An FDA advisory panel will meet to consider Medtronic's pre-market approval application for its DIAM spinal stabilization system, according to a Mass Device report.
Exactech's board of directors authorized a 1 million share buy back of company shares over the next two years.
The FDA cleared the Dyneema Purity Radiopaque Cerclage Cable by DSM Biomedical, an Exton, Penn.-based developer of biomedical materials and regenerative medicine.
Two vital devices to aid recovery during therapy for hand injuries or following surgery is now available.
Xtant Medical will have the first surgical case of the Atrix-C Cervical Allograft Interbody Spacer.
MEDTECH sold two new ROSA robotic surgery systems in the United States.
Plans underway to initiate the Cervical IDE for the Freedom Disc in the USA
Quentin Blackford, CFO and chief administrative officer of NuVasive, sold a total of 15,000 shares of the company, according to a Financial Magazin report.
