ArthroCare Receives FDA 510(k) Clearance for 6.5 Spartan Needle Anchor

ArthroCare, an Austin, Texas-based minimally invasive surgical products company, received FDA clearance for its 6.5 Spartan needle anchor, according to a company news release.

Advertisement

The devices are a preloaded threaded anchor indicated for use during fixation of soft tissue to bone. The needle version can be utilized during open repairs, while the previously cleared non-needle version is used for arthroscopic repairs.

The 6.5mm screw-in design can be used during single or double row repairs.

Read the report on Spartan.

Related Articles on ArthroCare:

ArthroCare Total Revenue Increases by 10.6% to %$7.9M
ArthroCare Receives FDA 510(k) Clearance for Suture Implant System
ArhtoCare Launches Device Collection for Temperature Monitoring During Arthrosocpy

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.