FDA 510(k) clearance received for HA-enhanced Tactoset Injectable Bone Substitute for the treatment of insufficiency fractures.
501(k) clearance received for Slik Knotless Screw-In Suture Anchors and Slik Fix Tenodesis System2.
FDA 510(k) clearance received for HA-enhanced Tactoset Injectable Bone Substitute for the treatment of insufficiency fractures.
501(k) clearance received for Slik Knotless Screw-In Suture Anchors and Slik Fix Tenodesis System2.