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Zimmer Biomet Holdings Inc. has announced FDA 510(k) clearance of its Persona OsseoTi keel tibia for patients undergoing cementless total knee replacement, according to a company press release.The Persona OsseoTi includes a porous version of the Persona anatomic tibia with porous metal technology for biological fixation, which uses 3D printing and anatomical data, according to the release.
-- New Porous Iteration of Anatomic Keeled Tibia Designed to Deliver Stable Initial and Biological Fixation Together with the Clinically Proven Be...
Zimmer Biomet (NYSE:ZBH) announced today that it received FDA 510(k) clearance for the Persona OsseoTi Keel Tibia.
Zimmer Biomet Inc. has announced FDA 510(k) clearance of the Identity shoulder system for anatomic, reverse and revision shoulder replacement procedures, according to a company press release.The Identity shoulder system is compatible with a range of humeral and glenoid options to fit each patient’s unique anatomy, according to the release.