Custom Spine Receives FDA 510(k) Clearance for Securis Cannulated Screw System

Custom Spine has announced it has received FDA 510(k) clearance for its Securis cannulated pedicle screw system, according to a news release.

Advertisement

 

The system is Custom Spine’s first entry into the minimally invasive spine market.

 

The Securis cannulated screw system features a chromium-cobalt rod and advanced instrumentation, according to the company.

 

“Custom Spine is excited about this upcoming release of the first of many minimally invasive solutions for spine surgeons,” said Mahmoud Abdelgany, president of Custom Spine, in the release. “The FDA clearance of Securis represents the successful completion of another milestone for the company and supports our future growth plans.”

 

Related Articles on Minimally Invasive Spine:

207 Spine Surgeons & Specialists to Know

One Spine Surgeon’s Journey to Profitability: 5 Points on Dr. Anthony Yeung’s Unique Practice & Procedure

5 Trends in Pain Management With Dr. Ira Fox of the World Institute of Pain

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Advertisement

Next Up in Uncategorized

Advertisement

Comments are closed.