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.

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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

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