ArthroCare Receives FDA 510(k) Clearance for Suture Implant System

ArthroCare received FDA 510(k) clearance for the Spartan PEEK suture implant system, a preloaded PEEK threaded anchor for use in soft tissue to bone fixation, according to a company news release.

Advertisement

Spartan joins several other ArthroCare anchors that are compatible with ArthroCare suture passing technology. Spartan has a 5.5-mm screw-in design for stronger pull-out strength and can be used to perform single and double row repairs.

Read the ArthroCare release on Spartan PEEK.

Read other coverage on ArthroCare:

– ArthroCare Receives FDA Clearance for Vertebral Augmentation Device

– ArthroCare Launches Device Collection for Temperature Monitoring During Arthroscopy

– ArthroCare Picks 75-Year-Old Industry Veteran as Permanent CEO

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 Spinal Tech

Advertisement

Comments are closed.