Surgeons should understand the stages and indications for removal of retained hardware in total knee arthroplasty to avoid malpositioning, infection or the unnecessary removal of hardware ...

Of these, the researchers matched a cohort of 1962 patients who underwent outpatient TKA under general anesthesia with patients who underwent outpatient TKA under spinal anesthesia.

Monogram received FDA 510(k) clearance for its robotic-assisted total knee arthroplasty system, Monogram mBôs TKA. The company plans initial placements with key surgeons and aims to expand its ...

DiviTum® TKa has received FDA 510 (k) clearance in the US and is CE-marked in the EU. Biovica's shares are traded on the Nasdaq First North Premier Growth Market (BIOVIC B).

Monogram May Market the Monogram mBôs™ TKA System, Subject to the Requirements of the Federal Food, Drug, and Cosmetic Act (the Act). The Company is Preparing for Commercialization and ...

Biovica's assay, DiviTum® TKa, measures cell proliferation by detecting the TKa biomarker in the bloodstream. The assay has demonstrated its ability to provide insight to therapy effectiveness in ...