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.

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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

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